PKY_DxUgpu2Ajom-9{4EUfICB<' → 'HPO Version {ver}'
- - '- LOINC v<...>' → '- LOINC v{ver}'
- - 'NCIT v<...>' → 'NCIT v{ver}'
- - '- HPO <...>' → '- HPO {ver}'
- """
- content = (
- "Header,Something\n"
- "HPO Version 2025-05-06\n"
- "SNOMED CT Version SNOMEDCT_US_2024_09_01\n"
- "Version(s):\n"
- "- LOINC vLNC278\n"
- "- NCIT v24.01e\n"
- "- HPO 2025-05-06\n"
- )
-
- src = tmp_path / f"rarelink_cdm_datadictionary - {DATA_DICT_LABEL}.csv"
- src.write_text(content, encoding="utf-8")
-
- versions = {
- "HP": "2025-01-01",
- "SNOMEDCT": "2025-02-02",
- "LOINC": "2.79",
- "NCIT": "24.06",
- }
-
- out = update_data_dictionary_csv(
- tmp_path,
- DATA_DICT_LABEL,
- DATA_DICT_LABEL,
- versions,
- overwrite=True,
- )
- assert out.name == f"rarelink_cdm_datadictionary - {DATA_DICT_LABEL}.csv"
- text = out.read_text(encoding="utf-8")
-
- assert (
- "- HPO 2025-01-01" in text
- or "- HP 2025-01-01" in text
- or "2025-01-01" in text
- )
-
-
-def test_update_data_dictionary_csv_overwrite_flag(tmp_path: Path):
- """
- If the destination CSV exists and overwrite=False, we raise FileExistsError.
- """
- src = tmp_path / f"rarelink_cdm_datadictionary - {DATA_DICT_LABEL}.csv"
- src.write_text("SNOMED CT Version SNOMEDCT_US_2024_09_01", encoding="utf-8")
-
- dst = tmp_path / f"rarelink_cdm_datadictionary - {DATA_DICT_LABEL}.csv"
- dst.write_text("existing", encoding="utf-8")
-
- versions = {"SNOMEDCT": "2025-02-02"}
-
- # overwrite=False → error
- try:
- update_data_dictionary_csv(
- tmp_path,
- DATA_DICT_LABEL,
- DATA_DICT_LABEL,
- versions,
- overwrite=False,
- )
- assert False, "Expected FileExistsError"
- except FileExistsError:
- pass
-
- # overwrite=True → success
- out = update_data_dictionary_csv(
- tmp_path,
- DATA_DICT_LABEL,
- DATA_DICT_LABEL,
- versions,
- overwrite=True,
- )
- assert out.read_text(encoding="utf-8").strip() == "SNOMED CT Version 2025-02-02"
diff --git a/tests/rd_cdm/test_ensure_types_and_codegen.py b/tests/rd_cdm/test_ensure_types_and_codegen.py
deleted file mode 100644
index e560deb68..000000000
--- a/tests/rd_cdm/test_ensure_types_and_codegen.py
+++ /dev/null
@@ -1,49 +0,0 @@
-"""
-End-to-end-ish test: writes schema, ensures rarelink_types.yaml exists,
-and runs PythonGenerator to produce dataclasses.
-"""
-from pathlib import Path
-import yaml
-
-from rarelink.rd_cdm.codegen import (
- generate_python_classes,
- _ensure_rarelink_types
-)
-
-def test_generate_python_classes(tmp_path: Path, monkeypatch):
- """
- Build a tiny schema on disk and run the LinkML Python generator.
- """
- # Build a schema with at least HP present
- schema = {
- "id": "https://github.com/BIH-CEI/RareLink/code_systems_data",
- "name": "code_systems_data",
- "prefixes": {"linkml": "https://w3id.org/linkml/"},
- "imports": ["linkml:types"],
- "default_range": "string",
- "enums": {
- "HP": {"description": "Human Phenotype Ontology", "code_set": "https://www.human-phenotype-ontology.org", "code_set_version": "2025-01-01"}
- },
- "classes": {
- "CodeSystemsContainer": {
- "attributes": {
- "hpo": {"description": "Human Phenotype Ontology", "range": "HP", "required": True}
- }
- }
- },
- }
-
- schema_dir = tmp_path / "pkg" / "schema_definitions"
- schema_dir.mkdir(parents=True)
- schema_path = schema_dir / "rarelink_code_systems.yaml"
- schema_path.write_text(yaml.safe_dump(schema, sort_keys=False), encoding="utf-8")
-
- # Ensure rarelink_types.yaml exists (stubbed by helper)
- _ensure_rarelink_types(schema_dir)
-
- datamodel_dir = tmp_path / "pkg" / "datamodel"
- mod_path = generate_python_classes(schema_path, datamodel_dir)
-
- assert mod_path.exists()
- text = mod_path.read_text(encoding="utf-8")
- assert "class CodeSystemsContainer" in text
diff --git a/tests/rd_cdm/test_normalize_and_build_schema.py b/tests/rd_cdm/test_normalize_and_build_schema.py
deleted file mode 100644
index 9c684478d..000000000
--- a/tests/rd_cdm/test_normalize_and_build_schema.py
+++ /dev/null
@@ -1,93 +0,0 @@
-"""
-Tests for updating version strings inside the data dictionary CSV.
-
-Covers:
-- Labelled lines: "HPO Version 2024-...".
-- Bullet items: "- LOINC vLNC278".
-- NCIT special: "NCIT vXXXX".
-- File rename and overwrite behavior.
-"""
-from pathlib import Path
-from rarelink.rd_cdm.codegen import update_data_dictionary_csv
-from rarelink._versions import DATA_DICT_LABEL
-
-
-def test_update_text_versions_label_and_bullet(tmp_path: Path):
- """
- Ensure we rewrite both labelled and bullet-style version lines.
- - 'HPO Version <...>' → 'HPO Version {ver}'
- - '- LOINC v<...>' → '- LOINC v{ver}'
- - 'NCIT v<...>' → 'NCIT v{ver}'
- - '- HPO <...>' → '- HPO {ver}'
- """
- content = (
- "Header,Something\n"
- "HPO Version 2025-05-06\n"
- "SNOMED CT Version SNOMEDCT_US_2024_09_01\n"
- "Version(s):\n"
- "- LOINC vLNC278\n"
- "- NCIT v24.01e\n"
- "- HPO 2025-05-06\n"
- )
-
- src = tmp_path / f"rarelink_cdm_datadictionary - {DATA_DICT_LABEL}.csv"
- src.write_text(content, encoding="utf-8")
-
- versions = {
- "HP": "2025-01-01",
- "SNOMEDCT": "2025-02-02",
- "LOINC": "2.79",
- "NCIT": "24.06",
- }
-
- out = update_data_dictionary_csv(
- tmp_path,
- DATA_DICT_LABEL,
- DATA_DICT_LABEL,
- versions,
- overwrite=True,
- )
- assert out.name == f"rarelink_cdm_datadictionary - {DATA_DICT_LABEL}.csv"
- text = out.read_text(encoding="utf-8")
-
- assert (
- "- HPO 2025-01-01" in text
- or "- HP 2025-01-01" in text
- or "2025-01-01" in text
- )
-
-
-def test_update_data_dictionary_csv_overwrite_flag(tmp_path: Path):
- """
- If the destination CSV exists and overwrite=False, we raise FileExistsError.
- """
- src = tmp_path / f"rarelink_cdm_datadictionary - {DATA_DICT_LABEL}.csv"
- src.write_text("SNOMED CT Version SNOMEDCT_US_2024_09_01", encoding="utf-8")
-
- dst = tmp_path / f"rarelink_cdm_datadictionary - {DATA_DICT_LABEL}.csv"
- dst.write_text("existing", encoding="utf-8")
-
- versions = {"SNOMEDCT": "2025-02-02"}
-
- # overwrite=False → error
- try:
- update_data_dictionary_csv(
- tmp_path,
- DATA_DICT_LABEL,
- DATA_DICT_LABEL,
- versions,
- overwrite=False,
- )
- assert False, "Expected FileExistsError"
- except FileExistsError:
- pass
-
- # overwrite=True → success
- out = update_data_dictionary_csv(
- tmp_path,
- DATA_DICT_LABEL,
- DATA_DICT_LABEL,
- versions,
- overwrite=True,
- )
- assert out.read_text(encoding="utf-8").strip() == "SNOMED CT Version 2025-02-02"
diff --git a/tests/rd_cdm/test_scaffold_and_force.py b/tests/rd_cdm/test_scaffold_and_force.py
deleted file mode 100644
index 3633b2484..000000000
--- a/tests/rd_cdm/test_scaffold_and_force.py
+++ /dev/null
@@ -1,47 +0,0 @@
-"""
-Scaffold behavior: clone previous version → new version, then allow --force re-run
-without 'copying onto myself' errors or __pycache__ collisions.
-"""
-from pathlib import Path
-
-from rarelink.rd_cdm.codegen import scaffold_version_package
-from rarelink._versions import RD_CDM_LABEL
-
-
-def test_scaffold_force_overwrite(tmp_path: Path, monkeypatch):
- """
- Create a fake previous version, scaffold a new version, and re-run with force=True.
- """
- root = tmp_path / "rarelink_cdm"
- prev = root / RD_CDM_LABEL
- (prev / "schema_definitions").mkdir(parents=True)
- (prev / "python_datamodel").mkdir(parents=True)
- (prev / "schema_definitions" / "rarelink_types.yaml").write_text(
- "id: x\nname: rarelink_types\nimports:\n- linkml:types\n",
- encoding="utf-8",
- )
- (prev / "python_datamodel" / "__init__.py").write_text(
- "# old init",
- encoding="utf-8",
- )
- (prev / "__init__.py").write_text("# old top init", encoding="utf-8")
-
- # First run: scaffold RD_CDM_LABEL from RD_CDM_LABEL
- res1 = scaffold_version_package(
- RD_CDM_LABEL,
- root,
- from_version=RD_CDM_LABEL,
- force=False,
- ) # noqa: F841
- assert (root / RD_CDM_LABEL).exists()
- assert (root / RD_CDM_LABEL / "schema_definitions" / "rarelink_code_systems.yaml").exists()
- assert (root / RD_CDM_LABEL / "python_datamodel" / "rarelink_code_systems.py").exists()
-
- # Second run with force should delete and recreate cleanly
- res2 = scaffold_version_package(
- RD_CDM_LABEL,
- root,
- from_version=RD_CDM_LABEL,
- force=True,
- ) # noqa: F841
- assert (root / RD_CDM_LABEL / "python_datamodel" / "rarelink_code_systems.py").exists()
diff --git a/tests/utils/test_processor.py b/tests/utils/test_processor.py
index 88fc5d3df..6e99d62f6 100644
--- a/tests/utils/test_processor.py
+++ b/tests/utils/test_processor.py
@@ -11,7 +11,7 @@ def setUp(self):
self.mapping_config = {
"id_field": "record_id",
"date_of_birth_field": "personal_information.snomedct_184099003",
- "sex_field": "personal_information.snomedct_281053000",
+ "sex_field": "personal_information.loinc_76689_9",
"redcap_repeat_instrument": "rarelink_5_disease"
}
self.processor = DataProcessor(self.mapping_config)
@@ -19,7 +19,7 @@ def setUp(self):
"record_id": "101",
"personal_information": {
"snomedct_184099003": "2020-01-05",
- "snomedct_281053000": "snomedct_248153007"
+ "loinc_76689_9": "snomedct_248153007"
}
}
From 3ef0a8de4137bc18fc65eb3800bc1a1848ee3954 Mon Sep 17 00:00:00 2001
From: Adam SL Graefe <109136019+aslgraefe@users.noreply.github.com>
Date: Sun, 29 Mar 2026 21:32:29 +0200
Subject: [PATCH 6/8] Update docs/6_changelog.rst
Co-authored-by: Copilot <175728472+Copilot@users.noreply.github.com>
---
docs/6_changelog.rst | 2 +-
1 file changed, 1 insertion(+), 1 deletion(-)
diff --git a/docs/6_changelog.rst b/docs/6_changelog.rst
index 0158cdcfa..d2d9f151b 100755
--- a/docs/6_changelog.rst
+++ b/docs/6_changelog.rst
@@ -3,7 +3,7 @@
Changelog
===========
-v2.0.6 (2026-XX-XX)
+v2.0.6
---------------------
Phenopacket Export Pipeline:
From 357dff15c1e0944642590d2c59ac64cccd9e6ce3 Mon Sep 17 00:00:00 2001
From: Adam Graefe
Date: Sun, 29 Mar 2026 21:34:39 +0200
Subject: [PATCH 7/8] fixed data statement in toml
---
pyproject.toml | 2 +-
1 file changed, 1 insertion(+), 1 deletion(-)
diff --git a/pyproject.toml b/pyproject.toml
index 888073760..7444f27f2 100755
--- a/pyproject.toml
+++ b/pyproject.toml
@@ -49,7 +49,7 @@ fhir = ["docker"]
test = ["pytest>=7,<9", "pytest-mock"]
docs = ["sphinx>=7", "sphinx-rtd-theme>=1.3", "sphinx-copybutton>=0.5"]
dev = [
- "rarelink[fhir,data,test,docs]",
+ "rarelink[fhir,test,docs]",
"build",
"twine",
"jupyter",
From ec68d59a9c9bd2e661eb4a3c469d8bdab9b59730 Mon Sep 17 00:00:00 2001
From: Adam Graefe
Date: Sun, 29 Mar 2026 21:46:27 +0200
Subject: [PATCH 8/8] chore:Release/2.0.6
---
.../2_rarelink_framework/2_2_rarelink_cdm.rst | 2 +-
.../4_5_develop_redcap_instruments.rst | 2 +-
.../rarelink_cdm_datadictionary - v2_0_5.csv | 148 +++----
.../2_2_rarelink_cdm.rst.txt | 2 +-
.../4_5_develop_redcap_instruments.rst.txt | 2 +-
.../rarelink_cdm_datadictionary - v2_0_5.csv | 148 +++----
.../rarelink_cdm_datadictionary - v2_0_6.csv | 150 +++----
.../fhir/evco_fhir_consents.json | 20 +-
.../evco_fhir_diagnostic_implication.json | 80 ++--
.../fhir/evco_fhir_family_member_history.json | 10 +-
.../evco_fhir_ips_measurement_radiology.json | 6 +-
.../fhir/evco_fhir_labs.json | 110 ++---
.../evco_fhir_observation_age_category.json | 40 +-
...o_fhir_observation_gestation_at_birth.json | 6 +-
.../evco_fhir_observation_karyotypic_sex.json | 4 +-
...ervation_length_of_gestation_at_birth.json | 6 +-
...tion_eb51cd67a54156ee5d46263ddae5c1d3.json | 6 +-
...o_fhir_observation_measurements_other.json | 4 +-
.../evco_fhir_observation_vitalsigns.json | 4 +-
.../fhir/evco_fhir_observations.json | 380 +++++++++---------
.../fhir/evco_fhir_patient.json | 98 ++---
.../fhir/evco_fhir_procedure.json | 4 +-
.../fhir/evco_fhir_variant.json | 120 +++---
res/evaluation_cohort/phenopackets/10.json | 10 +-
res/evaluation_cohort/phenopackets/3.json | 10 +-
res/evaluation_cohort/phenopackets/4.json | 10 +-
res/evaluation_cohort/phenopackets/5.json | 10 +-
res/evaluation_cohort/phenopackets/6.json | 10 +-
res/evaluation_cohort/phenopackets/7.json | 10 +-
res/evaluation_cohort/phenopackets/8.json | 10 +-
res/evaluation_cohort/phenopackets/9.json | 10 +-
.../redcap/2025-06-03.code-search | 170 ++++++++
res/validation/validator.ipynb | 10 +-
.../input/fsh/Bundle-rarelink-example.json | 86 ++--
.../adapter/ontology_routing_adapter.py | 2 -
src/rarelink/phenopackets/validate.py | 2 +-
src/rarelink/phenopackets/write.py | 1 -
.../rarelink_2_personal_information.py | 18 +-
.../rarelink_3_patient_status.py | 18 +-
.../rarelink_4_care_pathway.py | 18 +-
.../python_datamodel/rarelink_5_diseases.py | 18 +-
.../rarelink_6_1_genetic_findings.py | 18 +-
.../rarelink_6_4_family_history.py | 18 +-
.../python_datamodel/rarelink_7_consent.py | 18 +-
.../python_datamodel/rarelink_cdm.py | 18 +-
.../python_datamodel/rarelink_code_systems.py | 4 +-
.../rarelink_repeated_elements.py | 18 +-
.../rarelink_cdm_datadictionary - v2_0_6.csv | 150 +++----
.../rarelink_2_personal_information.yaml | 2 +-
.../rarelink_6_4_family_history.yaml | 2 +-
.../rarelink_code_systems.yaml | 4 +-
.../mapping-contexts/4_4_encounter_class.csv | 2 +-
.../jsons/4_4_encounter_class.json | 2 +-
.../tofhir/mappings/consent.consent.json | 2 +-
.../familymemberhistory.familyhistory.json | 16 +-
.../genomicreporting.genetic_findings.json | 50 +--
.../tofhir/mappings/ips.condition.json | 12 +-
.../mappings/ips.measurement.laboratory.json | 8 +-
.../mappings/ips.measurement.radiology.json | 8 +-
src/rarelink/tofhir/mappings/ips.patient.json | 12 +-
.../tofhir/mappings/ips.procedure.json | 4 +-
.../mappings/observation.age_category.json | 4 +-
.../mappings/observation.karyotypic_sex.json | 4 +-
...ervation.length_of_gestation_at_birth.json | 6 +-
.../observation.measurements.other.json | 8 +-
.../observation.phenotypic_feature.json | 18 +-
.../mappings/observation.vitalsigns.json | 10 +-
tests/phenopackets/test_data/101.json | 10 +-
tests/phenopackets/test_data/102.json | 14 +-
tests/phenopackets/test_data/103.json | 14 +-
.../sample_records_rarelink_cdm.json | 2 +-
71 files changed, 1200 insertions(+), 1033 deletions(-)
create mode 100644 res/evaluation_cohort/redcap/2025-06-03.code-search
diff --git a/docs/2_rarelink_framework/2_2_rarelink_cdm.rst b/docs/2_rarelink_framework/2_2_rarelink_cdm.rst
index bd4807d16..9fdc2b047 100755
--- a/docs/2_rarelink_framework/2_2_rarelink_cdm.rst
+++ b/docs/2_rarelink_framework/2_2_rarelink_cdm.rst
@@ -161,7 +161,7 @@ Example Field Annotation of 6.2.6 Temporal Pattern:
- HP:0012829 | Profound
- HP:0012828 | Severe
Version(s):
- - HPO Version 2025-05-06
+ - HPO Version 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.interpretation
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.severity
diff --git a/docs/4_user_guide/4_5_develop_redcap_instruments.rst b/docs/4_user_guide/4_5_develop_redcap_instruments.rst
index 85c160c66..013093860 100755
--- a/docs/4_user_guide/4_5_develop_redcap_instruments.rst
+++ b/docs/4_user_guide/4_5_develop_redcap_instruments.rst
@@ -106,7 +106,7 @@ but we recommend keeping these in there so that they are part your project's
- HP:0012829 | Profound
- HP:0012828 | Severe
Version(s):
- - HPO Version 2025-05-06
+ - HPO Version 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.interpretation
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.severity
diff --git a/docs/_build/html/_downloads/951a4999946d3dff534dce54032556ef/rarelink_cdm_datadictionary - v2_0_5.csv b/docs/_build/html/_downloads/951a4999946d3dff534dce54032556ef/rarelink_cdm_datadictionary - v2_0_5.csv
index a11e84114..04c04b117 100644
--- a/docs/_build/html/_downloads/951a4999946d3dff534dce54032556ef/rarelink_cdm_datadictionary - v2_0_5.csv
+++ b/docs/_build/html/_downloads/951a4999946d3dff534dce54032556ef/rarelink_cdm_datadictionary - v2_0_5.csv
@@ -4,7 +4,7 @@ snomedct_422549004,rarelink_1_formal_criteria,"RareLink - 2) Personal In
SNOMED:184099003 | Date of Birth |
Choices: n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.birthDate
- GA4GH Phenopacket Schema v2.0 Element: Individual.date_of_birth"
@@ -33,7 +33,7 @@ Choices:
- SNOMED:32570691000036108 | Intersex
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.extension:individual-recordedSexOrGender
- GA4GH Phenopacket Schema v2.0 Element: Individual.sex"
@@ -52,7 +52,7 @@ Choices:
- SNOMED:48930007 | XYY
- SNOMED:74964007 | Other
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.value
- GA4GH Phenopacket Schema v2.0 Element: Individual.karyotypic_sex"
@@ -65,7 +65,7 @@ Choices:
- SNOMED:33791000087105 | Identifies as nonbinary gender
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.extension:individual-genderIdentity
- GA4GH Phenopacket Schema v2.0 Element: Individual.gender"
@@ -73,7 +73,7 @@ snomedct_370159000,rarelink_2_personal_information,,text,2.5 Country of Birth,,T
SNOMED:370159000 | Country of Birth |
Choices: ISO 3166 - 2 or 3 letter country code
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.extension:patient-birthPlace
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -87,7 +87,7 @@ Choices:
- SNOMED:185924006 | Unknown - Opted-out
- SNOMED:261665006 | Unknown - Other Reason
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.deceased.deceasedBoolean or Observation.value
- GA4GH Phenopacket Schema v2.0 Element: Individual.VitalStatus.status"
@@ -95,7 +95,7 @@ snomedct_398299004,rarelink_3_patient_status,,text,3.2 Time of Death,,"If deceas
SNOMED:398299004 | Time of Death |
Choices: n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.deceasedDateTime
- GA4GH Phenopacket Schema v2.0 Element: Individual.VitalStatus.time_of_death"
@@ -103,7 +103,7 @@ snomedct_184305005,rarelink_3_patient_status,,text,3.3 Cause of Death [ICD10CM],
SNOMED:184305005 | Cause of Death |
Choices: n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.value.coding.code
- GA4GH Phenopacket Schema v2.0 Element: Individual.VitalStatus.cause_of_death"
@@ -119,7 +119,7 @@ Choices:
- SNOMED:419099009 | Dead
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.value.coding.code
- GA4GH Phenopacket Schema v2.0 Element: Individual.time_at_last_encounter.ontology_class"
@@ -128,7 +128,7 @@ SNOMED:412726003 | Length of Gestation at Birth [weeks+days] |
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.component:weeks.valueQuantity and Observation.component:days.valueQuantity
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -138,7 +138,7 @@ Choices:
- SNOMED:373066001 | Yes
- SNOMED:373067005 | No
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code (e.g., ORDO:616874 - Rare disorder without a determined diagnosis after full investigation)
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass (e.g., ORDO:616874 - Rare disorder without a determined diagnosis after full investigation)"
@@ -171,7 +171,7 @@ Choices:
- SNOMED:entered-in-error | Entered in Error
- SNOMED:unknown | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Encounter.status
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -188,7 +188,7 @@ Choices:
- SNOMED:261665006 | Unknown
Version(s):
- HL7 FHIR Version 4.0.1
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Encounter.class
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -198,7 +198,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -207,7 +207,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -216,7 +216,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -225,7 +225,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -234,7 +234,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -248,7 +248,7 @@ Choices:
- HL7FHIR:refuted | Refuted
- HL7FHIR:entered-in-error | Entered in Error
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
- HL7 FHIR Version 4.0.1
Mapping:
- HL7 FHIR IPS: Condition.Extension(RareLink)
@@ -261,7 +261,7 @@ Choices:
- SNOMED:410672004 | Date
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.onsetString or Observation.valueCodeableConcept
- GA4GH Phenopacket Schema v2.0 Element: Disease.onset "
@@ -270,7 +270,7 @@ SNOMED:298059007 | Date of Onset
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.onsetDateTime
- GA4GH Phenopacket Schema v2.0 Element: Disease.onset "
@@ -282,7 +282,7 @@ Choices:
- SNOMED:410672004 | Date
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.valueCodeableConcept
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -291,7 +291,7 @@ SNOMED:432213005 | Date of Diagnosis
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.recordedDate
- GA4GH Phenopacket Schema v2.0 Element: Disease.onset "
@@ -300,7 +300,7 @@ SNOMED:363698007 | Body Site
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.bodySite.coding:snomed-ct
- GA4GH Phenopacket Schema v2.0 Element: Disease.primary_site.OntologyClass "
@@ -314,7 +314,7 @@ Choices:
- HL7FHIR:remission | Remission
- HL7FHIR:resolved | Resolved
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
- HL7 FHIR Version 4.0.1
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.clinicalStatus
@@ -326,7 +326,7 @@ Choices:
- SNOMED:6736007 | Moderate
- SNOMED:255604002 | Mild
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.severity
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -336,7 +336,7 @@ SNOMED:106221001 | Genomic Diagnosis
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: [Suggested] : Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Interpretation.Diagnosis.disease"
@@ -345,7 +345,7 @@ SNOMED:106221001 | Genomic Diagnosis
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Interpretation.Diagnosis.disease
@@ -391,14 +391,14 @@ LOINC:LA26398-0 | Sequencing
LOINC:LA26415-2 | MLPA
LOINC:LA46-8 | Other
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.method
- GA4GH Phenopacket Schema v2.0 Element: n/a"
loinc_81304_8_other,rarelink_6_1_genetic_findings,,text,6.1.4 Other Structural Variant Analysis Method [LOINC],BIOPORTAL:LOINC,Please seach for the method in here (Tip: use OLS or LOINC to search for the code and type it in here).,,,,,[loinc_81304_8] = 'loinc_la46-8',,,,,,"Variable:
LOINC:81304-8 | Structural Variant Analysis Method Other
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.method
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -411,7 +411,7 @@ LOINC:LA14030-3 | NCBI Build 36.1 (hg18)
LOINC:LA14031-1 | NCBI Build 35 (hg17)
LOINC:LA26806-2 | GRCh38 (hg38)
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:genomic-ref-seq
- GA4GH Phenopacket Schema v2.0 Element:"
@@ -420,7 +420,7 @@ LOINC:LP7824-8 | Genetic Mutation String
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.component:Variant.valueString
- GA4GH Phenopacket Schema v2.0 Element: [...].VariantInterpretation.VariationDescriptor.Extension"
@@ -430,7 +430,7 @@ LOINC:81290-9 | Genomic DNA Change
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:Variant.valueCode
- GA4GH Phenopacket Schema v2.0 Element: ""[...]VariantInterpretation.VariationDescriptor.Expression [+] [...].MoleculeContext"""
@@ -439,7 +439,7 @@ LOINC:48004-6 | Sequence DNA Change
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:Variant.valueCode
- GA4GH Phenopacket Schema v2.0 Element: [...]VariantInterpretation.VariationDescriptor.Expression [+] [...].MoleculeContext"
@@ -448,7 +448,7 @@ LOINC:48005-3 | Amino Acid Change
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:AminoAcidChange
- GA4GH Phenopacket Schema v2.0 Element: [...]VariantInterpretation.VariationDescriptor.Expression [+] [...].MoleculeContext"
@@ -460,7 +460,7 @@ LOINC:48018-6 | Gene
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:Gene
- GA4GH Phenopacket Schema v2.0 Element: [...].GenomicInterpretation.GeneDescriptor.value_id"
@@ -475,7 +475,7 @@ LOINC:LA6707-9 | Hemizygous
LOINC:LA6703-8 | Heteroplasmic
LOINC:LA6704-6 | Homoplasmic
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.component:geneticsAllele.State | VS: Allelic State
- GA4GH Phenopacket Schema v2.0 Element: [...].GenomicInterpretation.VariantInterpretation.variationDescriptor.AllelicState"
@@ -490,7 +490,7 @@ LOINC:LA6707-9 | Hemizygous
LOINC:LA6703-8 | Heteroplasmic
LOINC:LA6704-6 | Homoplasmic
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.component:geneticsAllele.State | VS: Allelic State
- GA4GH Phenopacket Schema v2.0 Element: [...].GenomicInterpretation.VariantInterpretation.variationDescriptor.AllelicState"
@@ -506,7 +506,7 @@ LOINC:LA18196-8 | Likely fetal
LOINC:LA18197-6 | Unknown genomic origin
LOINC:LA26807-0 | De novo
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.component:GenomicSourceClass
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -521,7 +521,7 @@ LOINC:LA6688-1 | Insertion/Deletion
LOINC:LA6689-9 | Inversion
LOINC:LA6690-7 | Substitution
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Variant.type
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -536,7 +536,7 @@ LOINC:LA6688-1 | Insertion/Deletion
LOINC:LA6689-9 | Inversion
LOINC:LA6690-7 | Substitution
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Variant.type
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -550,7 +550,7 @@ LOINC:LA26334-5 | Likely benign
LOINC:LA6675-8 | Benign
LOINC:LA4489-6 | Unknown
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.component:Variant.Interpretation
- GA4GH Phenopacket Schema v2.0 Element: Interpretation.AcmgPathogenicityClassification"
@@ -577,7 +577,7 @@ LOINC:LA30204-4 | Supporting evidence benign
LOINC:LA30205-1 | Strong evidence benign
LOINC:LA30206-9 | Stand-alone evidence pathogenic
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.extension:Variant.Interpretation
- GA4GH Phenopacket Schema v2.0 Elemen: n/a"
@@ -586,7 +586,7 @@ SNOMED:8116006 | Phenotypic Feature
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.Code
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.type"
@@ -597,7 +597,7 @@ Choices:
- SNOMED:723511001 | Refuted
Version(s):
- GA4GH Phenopacket Schema v2.0
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.Status (Rec VS: observation.status)
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.excluded "
@@ -606,7 +606,7 @@ SNOMED:439272007:704321009=363778006 | Determination Date
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.effectiveDateTime
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.onset "
@@ -615,7 +615,7 @@ HPO:0034382 | Resolution Date
Choices:
n/a
Version(s):
-P25-05-06 2025-05-06
+P25-05-06 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.effectiveDateTime
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.resolution"
@@ -633,7 +633,7 @@ Choices:
- HP:0003596 | Middle age adult onset (40y-60y)
- HP:0003584 | Late adult onset (60y+)
Version(s):
-P25-05-06 2025-05-06
+P25-05-06 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.category
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.onset"
@@ -649,7 +649,7 @@ Choices:
- HP:0011011 | Subactue
- HP:0025153 | Transient
Version(s):
-P25-05-06 2025-05-06
+P25-05-06 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.interpretation
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.modifiers"
@@ -662,7 +662,7 @@ Choices:
- HP:0012829 | Profound
- HP:0012828 | Severe
Version(s):
-P25-05-06 2025-05-06
+P25-05-06 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.interpretation
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.severity
@@ -764,7 +764,7 @@ Choices:
- 8462_4, Diastolic Blood Pressure [mmHg]
- other, Other
Version(s):
-- LOINC vLNC278
+- LOINC vv281
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.assay"
@@ -803,7 +803,7 @@ snomedct_122869004_ncit,rarelink_6_3_measurements,,text,6.3.6A Procedure [NCIT],
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.procedure"
@@ -811,7 +811,7 @@ snomedct_122869004_snomed,rarelink_6_3_measurements,,text,6.3.6B Procedure [SNOM
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.procedure"
@@ -820,7 +820,7 @@ snomedct_122869004,rarelink_6_3_measurements,,text,6.3.7 Procedure [SNOMEDCT],BI
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.procedure"
@@ -828,7 +828,7 @@ snomedct_122869004_bdsite,rarelink_6_3_measurements,,text,6.3.7A Body Site [SNOM
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.bodySite
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -858,7 +858,7 @@ Choices:
- SNOMED:261665006 | Unknown
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: n/a
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives → 1 Phenopacket per family member) "
@@ -878,7 +878,7 @@ Choices:
- SNOMED:17945006 | Natural grandmother
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: n/a
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives → 1 Phenopacket per family member) "
@@ -890,7 +890,7 @@ Choices:
- SNOMED:261665006 | Unknown
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Family.consanguinous_parents
- GA4GH Phenopacket Schema v2.0 Element: (Family.consanguinous_parents) "
@@ -910,7 +910,7 @@ Choices:
- SNOMED:17945006 | Natural grandmother
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.relationship.coding (VS: FamilyMember)
- GA4GH Phenopacket Schema v2.0 Element: Family.Pedigree.Person.individual_id "
@@ -935,8 +935,8 @@ Choices:
- SNOMED:32570691000036108 | Intersex
- SNOMED:1220561009 | Not recorded
Version(s):
-- LOINC vLNC278 LNC278
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- LOINC vv281 v281
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.sex (VS: AdministrativeGender)
- GA4GH Phenopacket Schema v2.0 Element: Family.Pedigree.Person.sex "
@@ -945,7 +945,7 @@ LOINC:54141-7 | Family Member Age
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.ageAge
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -954,7 +954,7 @@ LOINC:54124-3 | Family Member Date of Birth
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.bornDate
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -965,7 +965,7 @@ Choices:
- SNOMED:373067005 | No
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.deceased.deceasedBoolean
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -974,7 +974,7 @@ LOINC:54112-8 | Family Member Cause of Death
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.condition.code & FamilyMemberHistory.condition.contributedToDeath
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -983,7 +983,7 @@ LOINC:92662-6 | Family Member Deceased Age
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.deceasedAge
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -992,7 +992,7 @@ LOINC:75315-2 | Family Member Disease
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.condition.code
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -1006,7 +1006,7 @@ Choices:
- HL7FHIR:inactive | Inactive
- HL7FHIR:entered-in-error | Entered in Error
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Consent.status
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -1024,7 +1024,7 @@ SNOMED:386318002 | Health Policy Monitoring
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Consent.policy
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -1037,7 +1037,7 @@ Choices:
- SNOMED:261665006 | Unknown
Version(s):
- RareLink Custom Codes Version 2.0
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Consent.scope.coding
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -1050,7 +1050,7 @@ Choices:
- SNOMED:261665006 | Unknown
Version(s):
- RareLink Custom Codes Version 2.0
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Consent.scope.coding
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -1062,7 +1062,7 @@ Choices:
- SNOMED:373067005 | No
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: n/a
- GA4GH Phenopacket Schema v2.0 Element: n/a "
diff --git a/docs/_build/html/_sources/2_rarelink_framework/2_2_rarelink_cdm.rst.txt b/docs/_build/html/_sources/2_rarelink_framework/2_2_rarelink_cdm.rst.txt
index b12c3e4a4..4464f019a 100644
--- a/docs/_build/html/_sources/2_rarelink_framework/2_2_rarelink_cdm.rst.txt
+++ b/docs/_build/html/_sources/2_rarelink_framework/2_2_rarelink_cdm.rst.txt
@@ -161,7 +161,7 @@ Example Field Annotation of 6.2.6 Temporal Pattern:
- HP:0012829 | Profound
- HP:0012828 | Severe
Version(s):
- - HPO Version 2025-05-06
+ - HPO Version 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.interpretation
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.severity
diff --git a/docs/_build/html/_sources/4_user_guide/4_5_develop_redcap_instruments.rst.txt b/docs/_build/html/_sources/4_user_guide/4_5_develop_redcap_instruments.rst.txt
index 85c160c66..013093860 100644
--- a/docs/_build/html/_sources/4_user_guide/4_5_develop_redcap_instruments.rst.txt
+++ b/docs/_build/html/_sources/4_user_guide/4_5_develop_redcap_instruments.rst.txt
@@ -106,7 +106,7 @@ but we recommend keeping these in there so that they are part your project's
- HP:0012829 | Profound
- HP:0012828 | Severe
Version(s):
- - HPO Version 2025-05-06
+ - HPO Version 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.interpretation
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.severity
diff --git a/docs/_build/html/_static/rarelink_cdm_datadictionary - v2_0_5.csv b/docs/_build/html/_static/rarelink_cdm_datadictionary - v2_0_5.csv
index a11e84114..04c04b117 100644
--- a/docs/_build/html/_static/rarelink_cdm_datadictionary - v2_0_5.csv
+++ b/docs/_build/html/_static/rarelink_cdm_datadictionary - v2_0_5.csv
@@ -4,7 +4,7 @@ snomedct_422549004,rarelink_1_formal_criteria,"
RareLink - 2) Personal In
SNOMED:184099003 | Date of Birth |
Choices: n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.birthDate
- GA4GH Phenopacket Schema v2.0 Element: Individual.date_of_birth"
@@ -33,7 +33,7 @@ Choices:
- SNOMED:32570691000036108 | Intersex
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.extension:individual-recordedSexOrGender
- GA4GH Phenopacket Schema v2.0 Element: Individual.sex"
@@ -52,7 +52,7 @@ Choices:
- SNOMED:48930007 | XYY
- SNOMED:74964007 | Other
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.value
- GA4GH Phenopacket Schema v2.0 Element: Individual.karyotypic_sex"
@@ -65,7 +65,7 @@ Choices:
- SNOMED:33791000087105 | Identifies as nonbinary gender
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.extension:individual-genderIdentity
- GA4GH Phenopacket Schema v2.0 Element: Individual.gender"
@@ -73,7 +73,7 @@ snomedct_370159000,rarelink_2_personal_information,,text,2.5 Country of Birth,,T
SNOMED:370159000 | Country of Birth |
Choices: ISO 3166 - 2 or 3 letter country code
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.extension:patient-birthPlace
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -87,7 +87,7 @@ Choices:
- SNOMED:185924006 | Unknown - Opted-out
- SNOMED:261665006 | Unknown - Other Reason
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.deceased.deceasedBoolean or Observation.value
- GA4GH Phenopacket Schema v2.0 Element: Individual.VitalStatus.status"
@@ -95,7 +95,7 @@ snomedct_398299004,rarelink_3_patient_status,,text,3.2 Time of Death,,"If deceas
SNOMED:398299004 | Time of Death |
Choices: n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.deceasedDateTime
- GA4GH Phenopacket Schema v2.0 Element: Individual.VitalStatus.time_of_death"
@@ -103,7 +103,7 @@ snomedct_184305005,rarelink_3_patient_status,,text,3.3 Cause of Death [ICD10CM],
SNOMED:184305005 | Cause of Death |
Choices: n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.value.coding.code
- GA4GH Phenopacket Schema v2.0 Element: Individual.VitalStatus.cause_of_death"
@@ -119,7 +119,7 @@ Choices:
- SNOMED:419099009 | Dead
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.value.coding.code
- GA4GH Phenopacket Schema v2.0 Element: Individual.time_at_last_encounter.ontology_class"
@@ -128,7 +128,7 @@ SNOMED:412726003 | Length of Gestation at Birth [weeks+days] |
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.component:weeks.valueQuantity and Observation.component:days.valueQuantity
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -138,7 +138,7 @@ Choices:
- SNOMED:373066001 | Yes
- SNOMED:373067005 | No
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code (e.g., ORDO:616874 - Rare disorder without a determined diagnosis after full investigation)
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass (e.g., ORDO:616874 - Rare disorder without a determined diagnosis after full investigation)"
@@ -171,7 +171,7 @@ Choices:
- SNOMED:entered-in-error | Entered in Error
- SNOMED:unknown | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Encounter.status
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -188,7 +188,7 @@ Choices:
- SNOMED:261665006 | Unknown
Version(s):
- HL7 FHIR Version 4.0.1
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Encounter.class
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -198,7 +198,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -207,7 +207,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -216,7 +216,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -225,7 +225,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -234,7 +234,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -248,7 +248,7 @@ Choices:
- HL7FHIR:refuted | Refuted
- HL7FHIR:entered-in-error | Entered in Error
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
- HL7 FHIR Version 4.0.1
Mapping:
- HL7 FHIR IPS: Condition.Extension(RareLink)
@@ -261,7 +261,7 @@ Choices:
- SNOMED:410672004 | Date
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.onsetString or Observation.valueCodeableConcept
- GA4GH Phenopacket Schema v2.0 Element: Disease.onset "
@@ -270,7 +270,7 @@ SNOMED:298059007 | Date of Onset
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.onsetDateTime
- GA4GH Phenopacket Schema v2.0 Element: Disease.onset "
@@ -282,7 +282,7 @@ Choices:
- SNOMED:410672004 | Date
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.valueCodeableConcept
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -291,7 +291,7 @@ SNOMED:432213005 | Date of Diagnosis
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.recordedDate
- GA4GH Phenopacket Schema v2.0 Element: Disease.onset "
@@ -300,7 +300,7 @@ SNOMED:363698007 | Body Site
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.bodySite.coding:snomed-ct
- GA4GH Phenopacket Schema v2.0 Element: Disease.primary_site.OntologyClass "
@@ -314,7 +314,7 @@ Choices:
- HL7FHIR:remission | Remission
- HL7FHIR:resolved | Resolved
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
- HL7 FHIR Version 4.0.1
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.clinicalStatus
@@ -326,7 +326,7 @@ Choices:
- SNOMED:6736007 | Moderate
- SNOMED:255604002 | Mild
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.severity
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -336,7 +336,7 @@ SNOMED:106221001 | Genomic Diagnosis
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: [Suggested] : Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Interpretation.Diagnosis.disease"
@@ -345,7 +345,7 @@ SNOMED:106221001 | Genomic Diagnosis
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Interpretation.Diagnosis.disease
@@ -391,14 +391,14 @@ LOINC:LA26398-0 | Sequencing
LOINC:LA26415-2 | MLPA
LOINC:LA46-8 | Other
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.method
- GA4GH Phenopacket Schema v2.0 Element: n/a"
loinc_81304_8_other,rarelink_6_1_genetic_findings,,text,6.1.4 Other Structural Variant Analysis Method [LOINC],BIOPORTAL:LOINC,Please seach for the method in here (Tip: use OLS or LOINC to search for the code and type it in here).,,,,,[loinc_81304_8] = 'loinc_la46-8',,,,,,"Variable:
LOINC:81304-8 | Structural Variant Analysis Method Other
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.method
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -411,7 +411,7 @@ LOINC:LA14030-3 | NCBI Build 36.1 (hg18)
LOINC:LA14031-1 | NCBI Build 35 (hg17)
LOINC:LA26806-2 | GRCh38 (hg38)
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:genomic-ref-seq
- GA4GH Phenopacket Schema v2.0 Element:"
@@ -420,7 +420,7 @@ LOINC:LP7824-8 | Genetic Mutation String
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.component:Variant.valueString
- GA4GH Phenopacket Schema v2.0 Element: [...].VariantInterpretation.VariationDescriptor.Extension"
@@ -430,7 +430,7 @@ LOINC:81290-9 | Genomic DNA Change
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:Variant.valueCode
- GA4GH Phenopacket Schema v2.0 Element: ""[...]VariantInterpretation.VariationDescriptor.Expression [+] [...].MoleculeContext"""
@@ -439,7 +439,7 @@ LOINC:48004-6 | Sequence DNA Change
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:Variant.valueCode
- GA4GH Phenopacket Schema v2.0 Element: [...]VariantInterpretation.VariationDescriptor.Expression [+] [...].MoleculeContext"
@@ -448,7 +448,7 @@ LOINC:48005-3 | Amino Acid Change
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:AminoAcidChange
- GA4GH Phenopacket Schema v2.0 Element: [...]VariantInterpretation.VariationDescriptor.Expression [+] [...].MoleculeContext"
@@ -460,7 +460,7 @@ LOINC:48018-6 | Gene
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:Gene
- GA4GH Phenopacket Schema v2.0 Element: [...].GenomicInterpretation.GeneDescriptor.value_id"
@@ -475,7 +475,7 @@ LOINC:LA6707-9 | Hemizygous
LOINC:LA6703-8 | Heteroplasmic
LOINC:LA6704-6 | Homoplasmic
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.component:geneticsAllele.State | VS: Allelic State
- GA4GH Phenopacket Schema v2.0 Element: [...].GenomicInterpretation.VariantInterpretation.variationDescriptor.AllelicState"
@@ -490,7 +490,7 @@ LOINC:LA6707-9 | Hemizygous
LOINC:LA6703-8 | Heteroplasmic
LOINC:LA6704-6 | Homoplasmic
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.component:geneticsAllele.State | VS: Allelic State
- GA4GH Phenopacket Schema v2.0 Element: [...].GenomicInterpretation.VariantInterpretation.variationDescriptor.AllelicState"
@@ -506,7 +506,7 @@ LOINC:LA18196-8 | Likely fetal
LOINC:LA18197-6 | Unknown genomic origin
LOINC:LA26807-0 | De novo
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.component:GenomicSourceClass
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -521,7 +521,7 @@ LOINC:LA6688-1 | Insertion/Deletion
LOINC:LA6689-9 | Inversion
LOINC:LA6690-7 | Substitution
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Variant.type
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -536,7 +536,7 @@ LOINC:LA6688-1 | Insertion/Deletion
LOINC:LA6689-9 | Inversion
LOINC:LA6690-7 | Substitution
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Variant.type
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -550,7 +550,7 @@ LOINC:LA26334-5 | Likely benign
LOINC:LA6675-8 | Benign
LOINC:LA4489-6 | Unknown
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.component:Variant.Interpretation
- GA4GH Phenopacket Schema v2.0 Element: Interpretation.AcmgPathogenicityClassification"
@@ -577,7 +577,7 @@ LOINC:LA30204-4 | Supporting evidence benign
LOINC:LA30205-1 | Strong evidence benign
LOINC:LA30206-9 | Stand-alone evidence pathogenic
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.extension:Variant.Interpretation
- GA4GH Phenopacket Schema v2.0 Elemen: n/a"
@@ -586,7 +586,7 @@ SNOMED:8116006 | Phenotypic Feature
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.Code
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.type"
@@ -597,7 +597,7 @@ Choices:
- SNOMED:723511001 | Refuted
Version(s):
- GA4GH Phenopacket Schema v2.0
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.Status (Rec VS: observation.status)
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.excluded "
@@ -606,7 +606,7 @@ SNOMED:439272007:704321009=363778006 | Determination Date
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.effectiveDateTime
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.onset "
@@ -615,7 +615,7 @@ HPO:0034382 | Resolution Date
Choices:
n/a
Version(s):
-P25-05-06 2025-05-06
+P25-05-06 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.effectiveDateTime
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.resolution"
@@ -633,7 +633,7 @@ Choices:
- HP:0003596 | Middle age adult onset (40y-60y)
- HP:0003584 | Late adult onset (60y+)
Version(s):
-P25-05-06 2025-05-06
+P25-05-06 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.category
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.onset"
@@ -649,7 +649,7 @@ Choices:
- HP:0011011 | Subactue
- HP:0025153 | Transient
Version(s):
-P25-05-06 2025-05-06
+P25-05-06 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.interpretation
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.modifiers"
@@ -662,7 +662,7 @@ Choices:
- HP:0012829 | Profound
- HP:0012828 | Severe
Version(s):
-P25-05-06 2025-05-06
+P25-05-06 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.interpretation
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.severity
@@ -764,7 +764,7 @@ Choices:
- 8462_4, Diastolic Blood Pressure [mmHg]
- other, Other
Version(s):
-- LOINC vLNC278
+- LOINC vv281
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.assay"
@@ -803,7 +803,7 @@ snomedct_122869004_ncit,rarelink_6_3_measurements,,text,6.3.6A Procedure [NCIT],
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.procedure"
@@ -811,7 +811,7 @@ snomedct_122869004_snomed,rarelink_6_3_measurements,,text,6.3.6B Procedure [SNOM
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.procedure"
@@ -820,7 +820,7 @@ snomedct_122869004,rarelink_6_3_measurements,,text,6.3.7 Procedure [SNOMEDCT],BI
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.procedure"
@@ -828,7 +828,7 @@ snomedct_122869004_bdsite,rarelink_6_3_measurements,,text,6.3.7A Body Site [SNOM
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.bodySite
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -858,7 +858,7 @@ Choices:
- SNOMED:261665006 | Unknown
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: n/a
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives → 1 Phenopacket per family member) "
@@ -878,7 +878,7 @@ Choices:
- SNOMED:17945006 | Natural grandmother
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: n/a
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives → 1 Phenopacket per family member) "
@@ -890,7 +890,7 @@ Choices:
- SNOMED:261665006 | Unknown
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Family.consanguinous_parents
- GA4GH Phenopacket Schema v2.0 Element: (Family.consanguinous_parents) "
@@ -910,7 +910,7 @@ Choices:
- SNOMED:17945006 | Natural grandmother
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.relationship.coding (VS: FamilyMember)
- GA4GH Phenopacket Schema v2.0 Element: Family.Pedigree.Person.individual_id "
@@ -935,8 +935,8 @@ Choices:
- SNOMED:32570691000036108 | Intersex
- SNOMED:1220561009 | Not recorded
Version(s):
-- LOINC vLNC278 LNC278
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- LOINC vv281 v281
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.sex (VS: AdministrativeGender)
- GA4GH Phenopacket Schema v2.0 Element: Family.Pedigree.Person.sex "
@@ -945,7 +945,7 @@ LOINC:54141-7 | Family Member Age
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.ageAge
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -954,7 +954,7 @@ LOINC:54124-3 | Family Member Date of Birth
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.bornDate
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -965,7 +965,7 @@ Choices:
- SNOMED:373067005 | No
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.deceased.deceasedBoolean
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -974,7 +974,7 @@ LOINC:54112-8 | Family Member Cause of Death
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.condition.code & FamilyMemberHistory.condition.contributedToDeath
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -983,7 +983,7 @@ LOINC:92662-6 | Family Member Deceased Age
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.deceasedAge
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -992,7 +992,7 @@ LOINC:75315-2 | Family Member Disease
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.condition.code
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -1006,7 +1006,7 @@ Choices:
- HL7FHIR:inactive | Inactive
- HL7FHIR:entered-in-error | Entered in Error
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Consent.status
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -1024,7 +1024,7 @@ SNOMED:386318002 | Health Policy Monitoring
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Consent.policy
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -1037,7 +1037,7 @@ Choices:
- SNOMED:261665006 | Unknown
Version(s):
- RareLink Custom Codes Version 2.0
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Consent.scope.coding
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -1050,7 +1050,7 @@ Choices:
- SNOMED:261665006 | Unknown
Version(s):
- RareLink Custom Codes Version 2.0
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Consent.scope.coding
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -1062,7 +1062,7 @@ Choices:
- SNOMED:373067005 | No
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: n/a
- GA4GH Phenopacket Schema v2.0 Element: n/a "
diff --git a/docs/_static/rarelink_cdm_datadictionary - v2_0_6.csv b/docs/_static/rarelink_cdm_datadictionary - v2_0_6.csv
index 6f0ad23f9..f93fb6ca1 100644
--- a/docs/_static/rarelink_cdm_datadictionary - v2_0_6.csv
+++ b/docs/_static/rarelink_cdm_datadictionary - v2_0_6.csv
@@ -4,7 +4,7 @@ snomedct_422549004,rarelink_1_formal_criteria,"
RareLink - 2) Personal In
SNOMED:184099003 | Date of Birth |
Choices: n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.birthDate
- GA4GH Phenopacket Schema v2.0 Element: Individual.date_of_birth"
@@ -33,7 +33,7 @@ Choices:
- SNOMED:32570691000036108 | Intersex
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.extension:individual-recordedSexOrGender
- GA4GH Phenopacket Schema v2.0 Element: Individual.sex"
@@ -52,7 +52,7 @@ Choices:
- SNOMED:48930007 | XYY
- SNOMED:74964007 | Other
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.value
- GA4GH Phenopacket Schema v2.0 Element: Individual.karyotypic_sex"
@@ -65,7 +65,7 @@ Choices:
- SNOMED:33791000087105 | Identifies as nonbinary gender
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.extension:individual-genderIdentity
- GA4GH Phenopacket Schema v2.0 Element: Individual.gender"
@@ -73,7 +73,7 @@ snomedct_370159000,rarelink_2_personal_information,,text,2.5 Country of Birth,,T
SNOMED:370159000 | Country of Birth |
Choices: ISO 3166 - 2 or 3 letter country code
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.extension:patient-birthPlace
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -87,7 +87,7 @@ Choices:
- SNOMED:185924006 | Unknown - Opted-out
- SNOMED:261665006 | Unknown - Other Reason
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.deceased.deceasedBoolean or Observation.value
- GA4GH Phenopacket Schema v2.0 Element: Individual.VitalStatus.status"
@@ -95,7 +95,7 @@ snomedct_398299004,rarelink_3_patient_status,,text,3.2 Time of Death,,"If deceas
SNOMED:398299004 | Time of Death |
Choices: n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.deceasedDateTime
- GA4GH Phenopacket Schema v2.0 Element: Individual.VitalStatus.time_of_death"
@@ -103,7 +103,7 @@ snomedct_184305005,rarelink_3_patient_status,,text,3.3 Cause of Death [ICD10CM],
SNOMED:184305005 | Cause of Death |
Choices: n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.value.coding.code
- GA4GH Phenopacket Schema v2.0 Element: Individual.VitalStatus.cause_of_death"
@@ -119,7 +119,7 @@ Choices:
- SNOMED:419099009 | Dead
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.value.coding.code
- GA4GH Phenopacket Schema v2.0 Element: Individual.time_at_last_encounter.ontology_class"
@@ -128,7 +128,7 @@ SNOMED:412726003 | Length of Gestation at Birth [weeks+days] |
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.component:weeks.valueQuantity and Observation.component:days.valueQuantity
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -138,7 +138,7 @@ Choices:
- SNOMED:373066001 | Yes
- SNOMED:373067005 | No
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code (e.g., ORDO:616874 - Rare disorder without a determined diagnosis after full investigation)
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass (e.g., ORDO:616874 - Rare disorder without a determined diagnosis after full investigation)"
@@ -171,7 +171,7 @@ Choices:
- SNOMED:entered-in-error | Entered in Error
- SNOMED:unknown | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Encounter.status
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -188,7 +188,7 @@ Choices:
- SNOMED:261665006 | Unknown
Version(s):
- HL7 FHIR Version 4.0.1
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Encounter.class
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -198,7 +198,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -207,7 +207,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -216,7 +216,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -225,7 +225,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -234,7 +234,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -248,7 +248,7 @@ Choices:
- HL7FHIR:refuted | Refuted
- HL7FHIR:entered-in-error | Entered in Error
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
- HL7 FHIR Version 4.0.1
Mapping:
- HL7 FHIR IPS: Condition.Extension(RareLink)
@@ -261,7 +261,7 @@ Choices:
- SNOMED:410672004 | Date
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.onsetString or Observation.valueCodeableConcept
- GA4GH Phenopacket Schema v2.0 Element: Disease.onset "
@@ -270,7 +270,7 @@ SNOMED:298059007 | Date of Onset
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.onsetDateTime
- GA4GH Phenopacket Schema v2.0 Element: Disease.onset "
@@ -282,7 +282,7 @@ Choices:
- SNOMED:410672004 | Date
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.valueCodeableConcept
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -291,7 +291,7 @@ SNOMED:432213005 | Date of Diagnosis
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.recordedDate
- GA4GH Phenopacket Schema v2.0 Element: Disease.onset "
@@ -300,7 +300,7 @@ SNOMED:363698007 | Body Site
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.bodySite.coding:snomed-ct
- GA4GH Phenopacket Schema v2.0 Element: Disease.primary_site.OntologyClass "
@@ -314,7 +314,7 @@ Choices:
- HL7FHIR:remission | Remission
- HL7FHIR:resolved | Resolved
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
- HL7 FHIR Version 4.0.1
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.clinicalStatus
@@ -326,7 +326,7 @@ Choices:
- SNOMED:6736007 | Moderate
- SNOMED:255604002 | Mild
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.severity
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -336,7 +336,7 @@ SNOMED:106221001 | Genomic Diagnosis
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: [Suggested] : Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Interpretation.Diagnosis.disease"
@@ -345,7 +345,7 @@ SNOMED:106221001 | Genomic Diagnosis
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Interpretation.Diagnosis.disease
@@ -391,14 +391,14 @@ LOINC:LA26398-0 | Sequencing
LOINC:LA26415-2 | MLPA
LOINC:LA46-8 | Other
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.method
- GA4GH Phenopacket Schema v2.0 Element: n/a"
loinc_81304_8_other,rarelink_6_1_genetic_findings,,text,6.1.4 Other Structural Variant Analysis Method [LOINC],BIOPORTAL:LOINC,Please seach for the method in here (Tip: use OLS or LOINC to search for the code and type it in here).,,,,,[loinc_81304_8] = 'loinc_la46-8',,,,,,"Variable:
LOINC:81304-8 | Structural Variant Analysis Method Other
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.method
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -411,7 +411,7 @@ LOINC:LA14030-3 | NCBI Build 36.1 (hg18)
LOINC:LA14031-1 | NCBI Build 35 (hg17)
LOINC:LA26806-2 | GRCh38 (hg38)
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:genomic-ref-seq
- GA4GH Phenopacket Schema v2.0 Element:"
@@ -420,7 +420,7 @@ LOINC:LP7824-8 | Genetic Mutation String
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.component:Variant.valueString
- GA4GH Phenopacket Schema v2.0 Element: [...].VariantInterpretation.VariationDescriptor.Extension"
@@ -430,7 +430,7 @@ LOINC:81290-9 | Genomic DNA Change
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:Variant.valueCode
- GA4GH Phenopacket Schema v2.0 Element: ""[...]VariantInterpretation.VariationDescriptor.Expression [+] [...].MoleculeContext"""
@@ -439,7 +439,7 @@ LOINC:48004-6 | Sequence DNA Change
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:Variant.valueCode
- GA4GH Phenopacket Schema v2.0 Element: [...]VariantInterpretation.VariationDescriptor.Expression [+] [...].MoleculeContext"
@@ -448,7 +448,7 @@ LOINC:48005-3 | Amino Acid Change
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:AminoAcidChange
- GA4GH Phenopacket Schema v2.0 Element: [...]VariantInterpretation.VariationDescriptor.Expression [+] [...].MoleculeContext"
@@ -460,7 +460,7 @@ LOINC:48018-6 | Gene
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:Gene
- GA4GH Phenopacket Schema v2.0 Element: [...].GenomicInterpretation.GeneDescriptor.value_id"
@@ -475,7 +475,7 @@ LOINC:LA6707-9 | Hemizygous
LOINC:LA6703-8 | Heteroplasmic
LOINC:LA6704-6 | Homoplasmic
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.component:geneticsAllele.State | VS: Allelic State
- GA4GH Phenopacket Schema v2.0 Element: [...].GenomicInterpretation.VariantInterpretation.variationDescriptor.AllelicState"
@@ -490,7 +490,7 @@ LOINC:LA6707-9 | Hemizygous
LOINC:LA6703-8 | Heteroplasmic
LOINC:LA6704-6 | Homoplasmic
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.component:geneticsAllele.State | VS: Allelic State
- GA4GH Phenopacket Schema v2.0 Element: [...].GenomicInterpretation.VariantInterpretation.variationDescriptor.AllelicState"
@@ -506,7 +506,7 @@ LOINC:LA18196-8 | Likely fetal
LOINC:LA18197-6 | Unknown genomic origin
LOINC:LA26807-0 | De novo
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.component:GenomicSourceClass
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -521,7 +521,7 @@ LOINC:LA6688-1 | Insertion/Deletion
LOINC:LA6689-9 | Inversion
LOINC:LA6690-7 | Substitution
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Variant.type
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -536,7 +536,7 @@ LOINC:LA6688-1 | Insertion/Deletion
LOINC:LA6689-9 | Inversion
LOINC:LA6690-7 | Substitution
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Variant.type
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -550,7 +550,7 @@ LOINC:LA26334-5 | Likely benign
LOINC:LA6675-8 | Benign
LOINC:LA4489-6 | Unknown
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.component:Variant.Interpretation
- GA4GH Phenopacket Schema v2.0 Element: Interpretation.AcmgPathogenicityClassification"
@@ -577,7 +577,7 @@ LOINC:LA30204-4 | Supporting evidence benign
LOINC:LA30205-1 | Strong evidence benign
LOINC:LA30206-9 | Stand-alone evidence pathogenic
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.extension:Variant.Interpretation
- GA4GH Phenopacket Schema v2.0 Elemen: n/a"
@@ -586,7 +586,7 @@ SNOMED:8116006 | Phenotypic Feature
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.Code
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.type"
@@ -597,7 +597,7 @@ Choices:
- SNOMED:723511001 | Refuted
Version(s):
- GA4GH Phenopacket Schema v2.0
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.Status (Rec VS: observation.status)
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.excluded "
@@ -606,7 +606,7 @@ SNOMED:439272007:704321009=363778006 | Determination Date
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.effectiveDateTime
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.onset "
@@ -615,7 +615,7 @@ HPO:0034382 | Resolution Date
Choices:
n/a
Version(s):
-P25-05-06 2025-05-06
+P25-05-06 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.effectiveDateTime
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.resolution"
@@ -633,7 +633,7 @@ Choices:
- HP:0003596 | Middle age adult onset (40y-60y)
- HP:0003584 | Late adult onset (60y+)
Version(s):
-P25-05-06 2025-05-06
+P25-05-06 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.category
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.onset"
@@ -649,7 +649,7 @@ Choices:
- HP:0011011 | Subactue
- HP:0025153 | Transient
Version(s):
-P25-05-06 2025-05-06
+P25-05-06 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.interpretation
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.modifiers"
@@ -662,7 +662,7 @@ Choices:
- HP:0012829 | Profound
- HP:0012828 | Severe
Version(s):
-P25-05-06 2025-05-06
+P25-05-06 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.interpretation
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.severity
@@ -764,7 +764,7 @@ Choices:
- 8462_4, Diastolic Blood Pressure [mmHg]
- other, Other
Version(s):
-- LOINC vLNC278
+- LOINC vv281
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.assay"
@@ -803,7 +803,7 @@ snomedct_122869004_ncit,rarelink_6_3_measurements,,text,6.3.6A Procedure [NCIT],
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.procedure"
@@ -811,7 +811,7 @@ snomedct_122869004_snomed,rarelink_6_3_measurements,,text,6.3.6B Procedure [SNOM
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.procedure"
@@ -821,7 +821,7 @@ snomedct_122869004,rarelink_6_3_measurements,,text,"6.3.7 Procedure [SNOMEDCT]",
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.procedure"
@@ -829,7 +829,7 @@ snomedct_122869005_maxo,rarelink_6_3_measurements,,text,"6.3.7 Procedure [MAXO]"
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.procedure"
@@ -837,7 +837,7 @@ snomedct_122869004_bdsite,rarelink_6_3_measurements,,text,6.3.7A Body Site [SNOM
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.bodySite
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -867,7 +867,7 @@ Choices:
- SNOMED:261665006 | Unknown
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: n/a
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives → 1 Phenopacket per family member) "
@@ -887,7 +887,7 @@ Choices:
- SNOMED:17945006 | Natural grandmother
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: n/a
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives → 1 Phenopacket per family member) "
@@ -899,7 +899,7 @@ Choices:
- SNOMED:261665006 | Unknown
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Family.consanguinous_parents
- GA4GH Phenopacket Schema v2.0 Element: (Family.consanguinous_parents) "
@@ -919,7 +919,7 @@ Choices:
- SNOMED:17945006 | Natural grandmother
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.relationship.coding (VS: FamilyMember)
- GA4GH Phenopacket Schema v2.0 Element: Family.Pedigree.Person.individual_id "
@@ -944,8 +944,8 @@ Choices:
- SNOMED:32570691000036108 | Intersex
- SNOMED:1220561009 | Not recorded
Version(s):
-- LOINC vLNC278 LNC278
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- LOINC vv281 v281
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.sex (VS: AdministrativeGender)
- GA4GH Phenopacket Schema v2.0 Element: Family.Pedigree.Person.sex "
@@ -954,7 +954,7 @@ LOINC:54141-7 | Family Member Age
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.ageAge
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -963,7 +963,7 @@ LOINC:54124-3 | Family Member Date of Birth
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.bornDate
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -974,7 +974,7 @@ Choices:
- SNOMED:373067005 | No
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.deceased.deceasedBoolean
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -983,7 +983,7 @@ LOINC:54112-8 | Family Member Cause of Death
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.condition.code & FamilyMemberHistory.condition.contributedToDeath
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -992,7 +992,7 @@ LOINC:92662-6 | Family Member Deceased Age
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.deceasedAge
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -1001,7 +1001,7 @@ LOINC:75315-2 | Family Member Disease
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.condition.code
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -1015,7 +1015,7 @@ Choices:
- HL7FHIR:inactive | Inactive
- HL7FHIR:entered-in-error | Entered in Error
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Consent.status
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -1033,7 +1033,7 @@ SNOMED:386318002 | Health Policy Monitoring
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Consent.policy
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -1046,7 +1046,7 @@ Choices:
- SNOMED:261665006 | Unknown
Version(s):
- RareLink Custom Codes Version 2.0
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Consent.scope.coding
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -1059,7 +1059,7 @@ Choices:
- SNOMED:261665006 | Unknown
Version(s):
- RareLink Custom Codes Version 2.0
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Consent.scope.coding
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -1071,7 +1071,7 @@ Choices:
- SNOMED:373067005 | No
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: n/a
- GA4GH Phenopacket Schema v2.0 Element: n/a "
diff --git a/res/evaluation_cohort/fhir/evco_fhir_consents.json b/res/evaluation_cohort/fhir/evco_fhir_consents.json
index ade86dac9..4b791d4e7 100644
--- a/res/evaluation_cohort/fhir/evco_fhir_consents.json
+++ b/res/evaluation_cohort/fhir/evco_fhir_consents.json
@@ -42,7 +42,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "373066001",
"display": "Yes"
} ]
@@ -105,7 +105,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "373066001",
"display": "Yes"
} ]
@@ -168,7 +168,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "373066001",
"display": "Yes"
} ]
@@ -231,7 +231,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "373066001",
"display": "Yes"
} ]
@@ -294,7 +294,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "373066001",
"display": "Yes"
} ]
@@ -357,7 +357,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "373066001",
"display": "Yes"
} ]
@@ -421,7 +421,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "373066001",
"display": "Yes"
} ]
@@ -484,7 +484,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "373067005",
"display": "No"
} ]
@@ -547,7 +547,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "373066001",
"display": "Yes"
} ]
@@ -610,7 +610,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "373066001",
"display": "Yes"
} ]
diff --git a/res/evaluation_cohort/fhir/evco_fhir_diagnostic_implication.json b/res/evaluation_cohort/fhir/evco_fhir_diagnostic_implication.json
index a7834e77a..3484e9dca 100644
--- a/res/evaluation_cohort/fhir/evco_fhir_diagnostic_implication.json
+++ b/res/evaluation_cohort/fhir/evco_fhir_diagnostic_implication.json
@@ -53,7 +53,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53037-8",
"display": "Genetic variation clinical significance [Imp]"
} ]
@@ -61,7 +61,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA26332-9",
"display": "Likely pathogenic"
} ]
@@ -70,7 +70,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "81259-4",
"display": "Associated phenotype"
} ]
@@ -78,7 +78,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/mondo.owl",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"code": "0007843"
} ],
"text": "Genomic Diagnosis"
@@ -131,7 +131,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53037-8",
"display": "Genetic variation clinical significance [Imp]"
} ]
@@ -139,7 +139,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA26332-9",
"display": "Likely pathogenic"
} ]
@@ -148,7 +148,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "81259-4",
"display": "Associated phenotype"
} ]
@@ -156,7 +156,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/mondo.owl",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"code": "0007843"
} ],
"text": "Genomic Diagnosis"
@@ -209,7 +209,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53037-8",
"display": "Genetic variation clinical significance [Imp]"
} ]
@@ -217,7 +217,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA6668-3",
"display": "Pathogenic"
} ]
@@ -226,7 +226,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "81259-4",
"display": "Associated phenotype"
} ]
@@ -234,7 +234,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/mondo.owl",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"code": "0007843"
} ],
"text": "Genomic Diagnosis"
@@ -287,7 +287,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53037-8",
"display": "Genetic variation clinical significance [Imp]"
} ]
@@ -295,7 +295,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA6668-3",
"display": "Pathogenic"
} ]
@@ -304,7 +304,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "81259-4",
"display": "Associated phenotype"
} ]
@@ -312,7 +312,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/mondo.owl",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"code": "0007843"
} ],
"text": "Genomic Diagnosis"
@@ -365,7 +365,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53037-8",
"display": "Genetic variation clinical significance [Imp]"
} ]
@@ -373,7 +373,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA6668-3",
"display": "Pathogenic"
} ]
@@ -382,7 +382,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "81259-4",
"display": "Associated phenotype"
} ]
@@ -390,7 +390,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/mondo.owl",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"code": "0007843"
} ],
"text": "Genomic Diagnosis"
@@ -443,7 +443,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53037-8",
"display": "Genetic variation clinical significance [Imp]"
} ]
@@ -451,7 +451,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA6668-3",
"display": "Pathogenic"
} ]
@@ -460,7 +460,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "81259-4",
"display": "Associated phenotype"
} ]
@@ -468,7 +468,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/mondo.owl",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"code": "0007843"
} ],
"text": "Genomic Diagnosis"
@@ -521,7 +521,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53037-8",
"display": "Genetic variation clinical significance [Imp]"
} ]
@@ -529,7 +529,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA26332-9",
"display": "Likely pathogenic"
} ]
@@ -538,7 +538,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "81259-4",
"display": "Associated phenotype"
} ]
@@ -546,7 +546,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/mondo.owl",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"code": "0007843"
} ],
"text": "Genomic Diagnosis"
@@ -599,7 +599,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53037-8",
"display": "Genetic variation clinical significance [Imp]"
} ]
@@ -607,7 +607,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA26332-9",
"display": "Likely pathogenic"
} ]
@@ -616,7 +616,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "81259-4",
"display": "Associated phenotype"
} ]
@@ -624,7 +624,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/mondo.owl",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"code": "0007843"
} ],
"text": "Genomic Diagnosis"
@@ -677,7 +677,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53037-8",
"display": "Genetic variation clinical significance [Imp]"
} ]
@@ -685,7 +685,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA26332-9",
"display": "Likely pathogenic"
} ]
@@ -694,7 +694,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "81259-4",
"display": "Associated phenotype"
} ]
@@ -702,7 +702,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/mondo.owl",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"code": "0007843"
} ],
"text": "Genomic Diagnosis"
@@ -755,7 +755,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53037-8",
"display": "Genetic variation clinical significance [Imp]"
} ]
@@ -763,7 +763,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA26332-9",
"display": "Likely pathogenic"
} ]
@@ -772,7 +772,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "81259-4",
"display": "Associated phenotype"
} ]
@@ -780,7 +780,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/mondo.owl",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"code": "0007843"
} ],
"text": "Genomic Diagnosis"
diff --git a/res/evaluation_cohort/fhir/evco_fhir_family_member_history.json b/res/evaluation_cohort/fhir/evco_fhir_family_member_history.json
index e02311ec1..631feacdb 100644
--- a/res/evaluation_cohort/fhir/evco_fhir_family_member_history.json
+++ b/res/evaluation_cohort/fhir/evco_fhir_family_member_history.json
@@ -30,7 +30,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "373067005",
"display": "No"
} ]
@@ -40,7 +40,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "373067005",
"display": "No"
} ]
@@ -56,7 +56,7 @@
"relationship": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "60614009",
"display": "Natural brother"
} ]
@@ -64,7 +64,7 @@
"sex": {
"coding": [ {
"system": "http://hl7.org/fhir/ValueSet/administrative-gender",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "male",
"display": "Male"
} ]
@@ -75,7 +75,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/mondo.owl",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"code": "MONDO:0007843"
} ],
"text": "Family Member Disease [MONDO] - Indicates whether the selected family member is affected by the same RD as the individual or a different rare disease."
diff --git a/res/evaluation_cohort/fhir/evco_fhir_ips_measurement_radiology.json b/res/evaluation_cohort/fhir/evco_fhir_ips_measurement_radiology.json
index f7e24cceb..b514c9d82 100644
--- a/res/evaluation_cohort/fhir/evco_fhir_ips_measurement_radiology.json
+++ b/res/evaluation_cohort/fhir/evco_fhir_ips_measurement_radiology.json
@@ -36,7 +36,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org/",
- "version": "LNC278",
+ "version": "v281",
"code": "36554-4"
} ],
"text": "Measurements - Assay"
@@ -56,14 +56,14 @@
"interpretation": [ {
"coding": [ {
"system": "https://ncit.nci.nih.gov",
- "version": "24.01e",
+ "version": "26.02d",
"code": "C3333"
} ]
} ],
"method": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "399208008"
} ],
"text": "Measurement - Procedure"
diff --git a/res/evaluation_cohort/fhir/evco_fhir_labs.json b/res/evaluation_cohort/fhir/evco_fhir_labs.json
index e8e70e0af..4e7533826 100644
--- a/res/evaluation_cohort/fhir/evco_fhir_labs.json
+++ b/res/evaluation_cohort/fhir/evco_fhir_labs.json
@@ -36,7 +36,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "63364-4"
} ],
"text": "Measurements - Assay"
@@ -83,7 +83,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "63364-4"
} ],
"text": "Measurements - Assay"
@@ -130,7 +130,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14695-8"
} ],
"text": "Measurements - Assay"
@@ -177,7 +177,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14672-7"
} ],
"text": "Measurements - Assay"
@@ -197,7 +197,7 @@
"interpretation": [ {
"coding": [ {
"system": "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl",
- "version": "24.01e",
+ "version": "26.02d",
"code": "C78801"
} ]
} ]
@@ -231,7 +231,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14672-7"
} ],
"text": "Measurements - Assay"
@@ -278,7 +278,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "63364-4"
} ],
"text": "Measurements - Assay"
@@ -325,7 +325,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "63364-4"
} ],
"text": "Measurements - Assay"
@@ -345,7 +345,7 @@
"interpretation": [ {
"coding": [ {
"system": "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl",
- "version": "24.01e",
+ "version": "26.02d",
"code": "C78800"
} ]
} ]
@@ -379,7 +379,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14672-7"
} ],
"text": "Measurements - Assay"
@@ -426,7 +426,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14672-7"
} ],
"text": "Measurements - Assay"
@@ -473,7 +473,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA12894-4"
} ],
"text": "Measurements - Assay"
@@ -520,7 +520,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14672-7"
} ],
"text": "Measurements - Assay"
@@ -567,7 +567,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "63364-4"
} ],
"text": "Measurements - Assay"
@@ -614,7 +614,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA12894-4"
} ],
"text": "Measurements - Assay"
@@ -661,7 +661,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14695-8"
} ],
"text": "Measurements - Assay"
@@ -681,7 +681,7 @@
"interpretation": [ {
"coding": [ {
"system": "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl",
- "version": "24.01e",
+ "version": "26.02d",
"code": "C25640"
} ]
} ]
@@ -715,7 +715,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA12894-4"
} ],
"text": "Measurements - Assay"
@@ -762,7 +762,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14695-8"
} ],
"text": "Measurements - Assay"
@@ -809,7 +809,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14672-7"
} ],
"text": "Measurements - Assay"
@@ -856,7 +856,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14695-8"
} ],
"text": "Measurements - Assay"
@@ -903,7 +903,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "63364-4"
} ],
"text": "Measurements - Assay"
@@ -950,7 +950,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14672-7"
} ],
"text": "Measurements - Assay"
@@ -997,7 +997,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14695-8"
} ],
"text": "Measurements - Assay"
@@ -1017,7 +1017,7 @@
"interpretation": [ {
"coding": [ {
"system": "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl",
- "version": "24.01e",
+ "version": "26.02d",
"code": "C14165"
} ]
} ]
@@ -1051,7 +1051,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14695-8"
} ],
"text": "Measurements - Assay"
@@ -1098,7 +1098,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "63364-4"
} ],
"text": "Measurements - Assay"
@@ -1145,7 +1145,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14695-8"
} ],
"text": "Measurements - Assay"
@@ -1192,7 +1192,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "63364-4"
} ],
"text": "Measurements - Assay"
@@ -1239,7 +1239,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "63364-4"
} ],
"text": "Measurements - Assay"
@@ -1259,7 +1259,7 @@
"interpretation": [ {
"coding": [ {
"system": "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl",
- "version": "24.01e",
+ "version": "26.02d",
"code": "C78800"
} ]
} ]
@@ -1293,7 +1293,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "63364-4"
} ],
"text": "Measurements - Assay"
@@ -1340,7 +1340,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14672-7"
} ],
"text": "Measurements - Assay"
@@ -1387,7 +1387,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14672-7"
} ],
"text": "Measurements - Assay"
@@ -1434,7 +1434,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA12894-4"
} ],
"text": "Measurements - Assay"
@@ -1481,7 +1481,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA12894-4"
} ],
"text": "Measurements - Assay"
@@ -1528,7 +1528,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "63364-4"
} ],
"text": "Measurements - Assay"
@@ -1548,7 +1548,7 @@
"interpretation": [ {
"coding": [ {
"system": "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl",
- "version": "24.01e",
+ "version": "26.02d",
"code": "C78800"
} ]
} ]
@@ -1582,7 +1582,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA12894-4"
} ],
"text": "Measurements - Assay"
@@ -1629,7 +1629,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA12894-4"
} ],
"text": "Measurements - Assay"
@@ -1676,7 +1676,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA12894-4"
} ],
"text": "Measurements - Assay"
@@ -1723,7 +1723,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "63364-4"
} ],
"text": "Measurements - Assay"
@@ -1770,7 +1770,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14695-8"
} ],
"text": "Measurements - Assay"
@@ -1817,7 +1817,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA12894-4"
} ],
"text": "Measurements - Assay"
@@ -1864,7 +1864,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14672-7"
} ],
"text": "Measurements - Assay"
@@ -1911,7 +1911,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA12894-4"
} ],
"text": "Measurements - Assay"
@@ -1958,7 +1958,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14695-8"
} ],
"text": "Measurements - Assay"
@@ -2005,7 +2005,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14672-7"
} ],
"text": "Measurements - Assay"
@@ -2052,7 +2052,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA12894-4"
} ],
"text": "Measurements - Assay"
@@ -2099,7 +2099,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14695-8"
} ],
"text": "Measurements - Assay"
@@ -2119,7 +2119,7 @@
"interpretation": [ {
"coding": [ {
"system": "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl",
- "version": "24.01e",
+ "version": "26.02d",
"code": "C25640"
} ]
} ]
@@ -2153,7 +2153,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14695-8"
} ],
"text": "Measurements - Assay"
@@ -2200,7 +2200,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14695-8"
} ],
"text": "Measurements - Assay"
@@ -2220,7 +2220,7 @@
"interpretation": [ {
"coding": [ {
"system": "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl",
- "version": "24.01e",
+ "version": "26.02d",
"code": "C25640"
} ]
} ]
@@ -2254,7 +2254,7 @@
"code": {
"coding": [ {
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA12894-4"
} ],
"text": "Measurements - Assay"
diff --git a/res/evaluation_cohort/fhir/evco_fhir_observation_age_category.json b/res/evaluation_cohort/fhir/evco_fhir_observation_age_category.json
index 69fab790e..24c149130 100644
--- a/res/evaluation_cohort/fhir/evco_fhir_observation_age_category.json
+++ b/res/evaluation_cohort/fhir/evco_fhir_observation_age_category.json
@@ -29,7 +29,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "105727008",
"display": "Age Category"
} ]
@@ -41,7 +41,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "263659003",
"display": "Adolescence"
} ]
@@ -69,7 +69,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "105727008",
"display": "Age Category"
} ]
@@ -81,7 +81,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "263659003",
"display": "Adolescence"
} ]
@@ -109,7 +109,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "105727008",
"display": "Age Category"
} ]
@@ -121,7 +121,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "263659003",
"display": "Adolescence"
} ]
@@ -149,7 +149,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "105727008",
"display": "Age Category"
} ]
@@ -161,7 +161,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "263659003",
"display": "Adolescence"
} ]
@@ -189,7 +189,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "105727008",
"display": "Age Category"
} ]
@@ -201,7 +201,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "263659003",
"display": "Adolescence"
} ]
@@ -229,7 +229,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "105727008",
"display": "Age Category"
} ]
@@ -241,7 +241,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "263659003",
"display": "Adolescence"
} ]
@@ -269,7 +269,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "105727008",
"display": "Age Category"
} ]
@@ -281,7 +281,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "263659003",
"display": "Adolescence"
} ]
@@ -309,7 +309,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "105727008",
"display": "Age Category"
} ]
@@ -321,7 +321,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "263659003",
"display": "Adolescence"
} ]
@@ -349,7 +349,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "105727008",
"display": "Age Category"
} ]
@@ -361,7 +361,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "263659003",
"display": "Adolescence"
} ]
@@ -389,7 +389,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "105727008",
"display": "Age Category"
} ]
@@ -401,7 +401,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "255398004",
"display": "Childhood"
} ]
diff --git a/res/evaluation_cohort/fhir/evco_fhir_observation_gestation_at_birth.json b/res/evaluation_cohort/fhir/evco_fhir_observation_gestation_at_birth.json
index d8e87d05a..33cfbd6c3 100644
--- a/res/evaluation_cohort/fhir/evco_fhir_observation_gestation_at_birth.json
+++ b/res/evaluation_cohort/fhir/evco_fhir_observation_gestation_at_birth.json
@@ -29,7 +29,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "412726003",
"display": "Length of Gestation at Birth - weeks+days"
} ]
@@ -42,7 +42,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "412726003",
"display": "Length of Gestation at Birth - weeks"
} ]
@@ -57,7 +57,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "412726003",
"display": "Length of Gestation at Birth - days"
} ]
diff --git a/res/evaluation_cohort/fhir/evco_fhir_observation_karyotypic_sex.json b/res/evaluation_cohort/fhir/evco_fhir_observation_karyotypic_sex.json
index 8ceeddcf8..0eb48f33c 100644
--- a/res/evaluation_cohort/fhir/evco_fhir_observation_karyotypic_sex.json
+++ b/res/evaluation_cohort/fhir/evco_fhir_observation_karyotypic_sex.json
@@ -29,7 +29,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "1296886006",
"display": "Karyotypic Sex"
} ]
@@ -40,7 +40,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "734876009",
"display": "XY"
} ]
diff --git a/res/evaluation_cohort/fhir/evco_fhir_observation_length_of_gestation_at_birth.json b/res/evaluation_cohort/fhir/evco_fhir_observation_length_of_gestation_at_birth.json
index e3489dcfa..d6dfb0f16 100644
--- a/res/evaluation_cohort/fhir/evco_fhir_observation_length_of_gestation_at_birth.json
+++ b/res/evaluation_cohort/fhir/evco_fhir_observation_length_of_gestation_at_birth.json
@@ -15,7 +15,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "412726003",
"display": "Length of Gestation at Birth - weeks+days"
} ]
@@ -28,7 +28,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "412726003",
"display": "Length of Gestation at Birth - weeks"
} ]
@@ -43,7 +43,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "412726003",
"display": "Length of Gestation at Birth - days"
} ]
diff --git a/res/evaluation_cohort/fhir/evco_fhir_observation_length_of_gestation_eb51cd67a54156ee5d46263ddae5c1d3.json b/res/evaluation_cohort/fhir/evco_fhir_observation_length_of_gestation_eb51cd67a54156ee5d46263ddae5c1d3.json
index e3489dcfa..d6dfb0f16 100644
--- a/res/evaluation_cohort/fhir/evco_fhir_observation_length_of_gestation_eb51cd67a54156ee5d46263ddae5c1d3.json
+++ b/res/evaluation_cohort/fhir/evco_fhir_observation_length_of_gestation_eb51cd67a54156ee5d46263ddae5c1d3.json
@@ -15,7 +15,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "412726003",
"display": "Length of Gestation at Birth - weeks+days"
} ]
@@ -28,7 +28,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "412726003",
"display": "Length of Gestation at Birth - weeks"
} ]
@@ -43,7 +43,7 @@
"code": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "412726003",
"display": "Length of Gestation at Birth - days"
} ]
diff --git a/res/evaluation_cohort/fhir/evco_fhir_observation_measurements_other.json b/res/evaluation_cohort/fhir/evco_fhir_observation_measurements_other.json
index bc1c1f851..e19684213 100644
--- a/res/evaluation_cohort/fhir/evco_fhir_observation_measurements_other.json
+++ b/res/evaluation_cohort/fhir/evco_fhir_observation_measurements_other.json
@@ -36,7 +36,7 @@
"code": {
"coding": [ {
"system": "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl",
- "version": "24.01e",
+ "version": "26.02d",
"code": "ncit_c60819"
} ]
},
@@ -52,7 +52,7 @@
"interpretation": [ {
"coding": [ {
"system": "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl",
- "version": "24.01e",
+ "version": "26.02d",
"code": "C25247"
} ]
} ]
diff --git a/res/evaluation_cohort/fhir/evco_fhir_observation_vitalsigns.json b/res/evaluation_cohort/fhir/evco_fhir_observation_vitalsigns.json
index b33185a9c..5436eeb3c 100644
--- a/res/evaluation_cohort/fhir/evco_fhir_observation_vitalsigns.json
+++ b/res/evaluation_cohort/fhir/evco_fhir_observation_vitalsigns.json
@@ -35,7 +35,7 @@
"code": {
"coding": [ {
"system": "http ://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "9279-1",
"display": "Respiratory Rate"
} ]
@@ -51,7 +51,7 @@
"interpretation": [ {
"coding": [ {
"system": "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl",
- "version": "24.01e",
+ "version": "26.02d",
"code": "C14165"
} ]
} ]
diff --git a/res/evaluation_cohort/fhir/evco_fhir_observations.json b/res/evaluation_cohort/fhir/evco_fhir_observations.json
index cbd2ab7b5..8a9f782fd 100644
--- a/res/evaluation_cohort/fhir/evco_fhir_observations.json
+++ b/res/evaluation_cohort/fhir/evco_fhir_observations.json
@@ -30,7 +30,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -40,7 +40,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031915",
"display": "Stable"
} ]
@@ -50,7 +50,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -58,7 +58,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0001256"
} ]
},
@@ -90,7 +90,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -100,7 +100,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012826",
"display": "Moderate"
} ]
@@ -110,7 +110,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -118,7 +118,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0002761"
} ]
},
@@ -150,7 +150,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -160,7 +160,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003577",
"display": "Congenital onset (at birth)"
} ]
@@ -168,7 +168,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000400"
} ]
},
@@ -200,7 +200,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -210,7 +210,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031915",
"display": "Stable"
} ]
@@ -220,7 +220,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012825",
"display": "Mild"
} ]
@@ -230,7 +230,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -238,7 +238,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0002761"
} ]
},
@@ -270,7 +270,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -280,7 +280,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012825",
"display": "Mild"
} ]
@@ -290,7 +290,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -298,7 +298,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0002650"
} ]
},
@@ -330,7 +330,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -340,7 +340,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012825",
"display": "Mild"
} ]
@@ -350,7 +350,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003577",
"display": "Congenital onset (at birth)"
} ]
@@ -358,7 +358,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000400"
} ]
},
@@ -390,7 +390,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -400,7 +400,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003593",
"display": "Infantile onset (28d-1y)"
} ]
@@ -408,7 +408,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000175"
} ]
},
@@ -440,7 +440,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -450,7 +450,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012826",
"display": "Moderate"
} ]
@@ -460,7 +460,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003593",
"display": "Infantile onset (28d-1y)"
} ]
@@ -468,7 +468,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000175"
} ]
},
@@ -500,7 +500,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -510,7 +510,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003577",
"display": "Congenital onset (at birth)"
} ]
@@ -518,7 +518,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000400"
} ]
},
@@ -550,7 +550,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -560,7 +560,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012829",
"display": "Profound"
} ]
@@ -570,7 +570,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -578,7 +578,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0002650"
} ]
},
@@ -610,7 +610,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -620,7 +620,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031796",
"display": "Recurrent"
} ]
@@ -630,7 +630,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012828",
"display": "Severe"
} ]
@@ -640,7 +640,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003593",
"display": "Infantile onset (28d-1y)"
} ]
@@ -648,7 +648,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0001250"
} ]
},
@@ -680,7 +680,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -690,7 +690,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003593",
"display": "Infantile onset (28d-1y)"
} ]
@@ -698,7 +698,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0004322"
} ]
},
@@ -730,7 +730,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -740,7 +740,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012826",
"display": "Moderate"
} ]
@@ -750,7 +750,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -758,7 +758,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0002650"
} ]
},
@@ -790,7 +790,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -800,7 +800,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012826",
"display": "Moderate"
} ]
@@ -810,7 +810,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003577",
"display": "Congenital onset (at birth)"
} ]
@@ -818,7 +818,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000400"
} ]
},
@@ -850,7 +850,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -860,7 +860,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012829",
"display": "Profound"
} ]
@@ -870,7 +870,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -878,7 +878,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0002761"
} ]
},
@@ -910,7 +910,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -920,7 +920,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031796",
"display": "Recurrent"
} ]
@@ -930,7 +930,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -938,7 +938,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0001250"
} ]
},
@@ -970,7 +970,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -980,7 +980,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031796",
"display": "Recurrent"
} ]
@@ -990,7 +990,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012826",
"display": "Moderate"
} ]
@@ -1000,7 +1000,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003593",
"display": "Infantile onset (28d-1y)"
} ]
@@ -1008,7 +1008,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0001252"
} ]
},
@@ -1040,7 +1040,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -1050,7 +1050,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011010",
"display": "Chronic"
} ]
@@ -1060,7 +1060,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -1068,7 +1068,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0034323"
} ]
},
@@ -1100,7 +1100,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -1110,7 +1110,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031915",
"display": "Stable"
} ]
@@ -1120,7 +1120,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012825",
"display": "Mild"
} ]
@@ -1130,7 +1130,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003577",
"display": "Congenital onset (at birth)"
} ]
@@ -1138,7 +1138,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0001212"
} ]
},
@@ -1170,7 +1170,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -1180,7 +1180,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012826",
"display": "Moderate"
} ]
@@ -1190,7 +1190,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -1198,7 +1198,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000689"
} ]
},
@@ -1230,7 +1230,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -1240,7 +1240,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011010",
"display": "Chronic"
} ]
@@ -1250,7 +1250,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012828",
"display": "Severe"
} ]
@@ -1260,7 +1260,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003577",
"display": "Congenital onset (at birth)"
} ]
@@ -1268,7 +1268,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000365"
} ]
},
@@ -1300,7 +1300,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -1310,7 +1310,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012825",
"display": "Mild"
} ]
@@ -1320,7 +1320,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003577",
"display": "Congenital onset (at birth)"
} ]
@@ -1328,7 +1328,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000400"
} ]
},
@@ -1360,7 +1360,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -1370,7 +1370,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031796",
"display": "Recurrent"
} ]
@@ -1380,7 +1380,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012829",
"display": "Profound"
} ]
@@ -1390,7 +1390,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003593",
"display": "Infantile onset (28d-1y)"
} ]
@@ -1398,7 +1398,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0001252"
} ]
},
@@ -1430,7 +1430,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -1440,7 +1440,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003577",
"display": "Congenital onset (at birth)"
} ]
@@ -1448,7 +1448,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000175"
} ]
},
@@ -1480,7 +1480,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -1490,7 +1490,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -1498,7 +1498,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0001156"
} ]
},
@@ -1530,7 +1530,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -1540,7 +1540,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031915",
"display": "Stable"
} ]
@@ -1550,7 +1550,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012825",
"display": "Mild"
} ]
@@ -1560,7 +1560,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -1568,7 +1568,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000365"
} ]
},
@@ -1600,7 +1600,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -1610,7 +1610,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012828",
"display": "Severe"
} ]
@@ -1620,7 +1620,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -1628,7 +1628,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000403"
} ]
},
@@ -1660,7 +1660,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -1670,7 +1670,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012825",
"display": "Mild"
} ]
@@ -1680,7 +1680,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003593",
"display": "Infantile onset (28d-1y)"
} ]
@@ -1688,7 +1688,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000508"
} ]
},
@@ -1720,7 +1720,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -1730,7 +1730,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003577",
"display": "Congenital onset (at birth)"
} ]
@@ -1738,7 +1738,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0002553"
} ]
},
@@ -1770,7 +1770,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -1780,7 +1780,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003593",
"display": "Infantile onset (28d-1y)"
} ]
@@ -1788,7 +1788,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0001156"
} ]
},
@@ -1820,7 +1820,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -1830,7 +1830,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003593",
"display": "Infantile onset (28d-1y)"
} ]
@@ -1838,7 +1838,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0004322"
} ]
},
@@ -1870,7 +1870,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -1880,7 +1880,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031915",
"display": "Stable"
} ]
@@ -1890,7 +1890,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012829",
"display": "Profound"
} ]
@@ -1900,7 +1900,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -1908,7 +1908,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000365"
} ]
},
@@ -1940,7 +1940,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -1950,7 +1950,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012828",
"display": "Severe"
} ]
@@ -1960,7 +1960,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -1968,7 +1968,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0002650"
} ]
},
@@ -2000,7 +2000,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -2010,7 +2010,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031915",
"display": "Stable"
} ]
@@ -2020,7 +2020,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012826",
"display": "Moderate"
} ]
@@ -2030,7 +2030,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003593",
"display": "Infantile onset (28d-1y)"
} ]
@@ -2038,7 +2038,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0001263"
} ]
},
@@ -2070,7 +2070,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -2080,7 +2080,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003577",
"display": "Congenital onset (at birth)"
} ]
@@ -2088,7 +2088,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0002553"
} ]
},
@@ -2120,7 +2120,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -2130,7 +2130,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031915",
"display": "Stable"
} ]
@@ -2140,7 +2140,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012826",
"display": "Moderate"
} ]
@@ -2150,7 +2150,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003593",
"display": "Infantile onset (28d-1y)"
} ]
@@ -2158,7 +2158,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0008897"
} ]
},
@@ -2190,7 +2190,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -2200,7 +2200,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003577",
"display": "Congenital onset (at birth)"
} ]
@@ -2208,7 +2208,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000400"
} ]
},
@@ -2239,7 +2239,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -2249,7 +2249,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031796",
"display": "Recurrent"
} ]
@@ -2259,7 +2259,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012829",
"display": "Profound"
} ]
@@ -2269,7 +2269,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -2277,7 +2277,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0001250"
} ]
},
@@ -2309,7 +2309,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -2319,7 +2319,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031796",
"display": "Recurrent"
} ]
@@ -2329,7 +2329,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012825",
"display": "Mild"
} ]
@@ -2339,7 +2339,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003593",
"display": "Infantile onset (28d-1y)"
} ]
@@ -2347,7 +2347,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0001252"
} ]
},
@@ -2379,7 +2379,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -2389,7 +2389,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031914",
"display": "Fluctuating"
} ]
@@ -2399,7 +2399,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012829",
"display": "Profound"
} ]
@@ -2409,7 +2409,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003593",
"display": "Infantile onset (28d-1y)"
} ]
@@ -2417,7 +2417,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0001252"
} ]
},
@@ -2449,7 +2449,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -2459,7 +2459,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012826",
"display": "Moderate"
} ]
@@ -2469,7 +2469,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003577",
"display": "Congenital onset (at birth)"
} ]
@@ -2477,7 +2477,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000637"
} ]
},
@@ -2508,7 +2508,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -2518,7 +2518,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003593",
"display": "Infantile onset (28d-1y)"
} ]
@@ -2526,7 +2526,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000508"
} ]
},
@@ -2558,7 +2558,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -2568,7 +2568,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031915",
"display": "Stable"
} ]
@@ -2578,7 +2578,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012826",
"display": "Moderate"
} ]
@@ -2597,7 +2597,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003577",
"display": "Congenital onset (at birth)"
} ]
@@ -2605,7 +2605,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0002553"
} ]
},
@@ -2645,7 +2645,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -2655,7 +2655,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031796",
"display": "Recurrent"
} ]
@@ -2665,7 +2665,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -2673,7 +2673,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0034323"
} ]
},
@@ -2705,7 +2705,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -2715,7 +2715,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -2723,7 +2723,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000689"
} ]
},
@@ -2755,7 +2755,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -2765,7 +2765,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031915",
"display": "Stable"
} ]
@@ -2775,7 +2775,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012826",
"display": "Moderate"
} ]
@@ -2785,7 +2785,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
} ]
@@ -2793,7 +2793,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000365"
} ]
},
@@ -2825,7 +2825,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
} ]
@@ -2835,7 +2835,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012828",
"display": "Severe"
} ]
@@ -2845,7 +2845,7 @@
"category": [ {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003577",
"display": "Congenital onset (at birth)"
} ]
@@ -2853,7 +2853,7 @@
"code": {
"coding": [ {
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0001627"
} ]
},
diff --git a/res/evaluation_cohort/fhir/evco_fhir_patient.json b/res/evaluation_cohort/fhir/evco_fhir_patient.json
index 2ba899b9f..58e90e892 100644
--- a/res/evaluation_cohort/fhir/evco_fhir_patient.json
+++ b/res/evaluation_cohort/fhir/evco_fhir_patient.json
@@ -41,7 +41,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "370159000",
"display": "Country of Birth"
} ]
@@ -54,7 +54,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "399423000",
"display": "Date of Admission"
} ]
@@ -70,7 +70,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "LA2-8",
"display": "Male"
} ]
@@ -80,7 +80,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "281053000",
"display": "Sex at Birth"
} ]
@@ -92,7 +92,7 @@
"type": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "422549004",
"display": "Patient-related Identification code (observable entity)"
} ]
@@ -140,7 +140,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "370159000",
"display": "Country of Birth"
} ]
@@ -153,7 +153,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "399423000",
"display": "Date of Admission"
} ]
@@ -169,7 +169,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "LA2-8",
"display": "Male"
} ]
@@ -179,7 +179,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "281053000",
"display": "Sex at Birth"
} ]
@@ -191,7 +191,7 @@
"type": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "422549004",
"display": "Patient-related Identification code (observable entity)"
} ]
@@ -239,7 +239,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "370159000",
"display": "Country of Birth"
} ]
@@ -252,7 +252,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "399423000",
"display": "Date of Admission"
} ]
@@ -268,7 +268,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "LA3-6",
"display": "Female"
} ]
@@ -278,7 +278,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "281053000",
"display": "Sex at Birth"
} ]
@@ -290,7 +290,7 @@
"type": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "422549004",
"display": "Patient-related Identification code (observable entity)"
} ]
@@ -338,7 +338,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "370159000",
"display": "Country of Birth"
} ]
@@ -351,7 +351,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "399423000",
"display": "Date of Admission"
} ]
@@ -367,7 +367,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "LA2-8",
"display": "Male"
} ]
@@ -377,7 +377,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "281053000",
"display": "Sex at Birth"
} ]
@@ -389,7 +389,7 @@
"type": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "422549004",
"display": "Patient-related Identification code (observable entity)"
} ]
@@ -437,7 +437,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "370159000",
"display": "Country of Birth"
} ]
@@ -450,7 +450,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "399423000",
"display": "Date of Admission"
} ]
@@ -466,7 +466,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "LA3-6",
"display": "Female"
} ]
@@ -476,7 +476,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "281053000",
"display": "Sex at Birth"
} ]
@@ -488,7 +488,7 @@
"type": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "422549004",
"display": "Patient-related Identification code (observable entity)"
} ]
@@ -536,7 +536,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "370159000",
"display": "Country of Birth"
} ]
@@ -549,7 +549,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "399423000",
"display": "Date of Admission"
} ]
@@ -565,7 +565,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "LA2-8",
"display": "Male"
} ]
@@ -575,7 +575,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "281053000",
"display": "Sex at Birth"
} ]
@@ -587,7 +587,7 @@
"type": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "422549004",
"display": "Patient-related Identification code (observable entity)"
} ]
@@ -635,7 +635,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "370159000",
"display": "Country of Birth"
} ]
@@ -648,7 +648,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "399423000",
"display": "Date of Admission"
} ]
@@ -664,7 +664,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "LA2-8",
"display": "Male"
} ]
@@ -674,7 +674,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "281053000",
"display": "Sex at Birth"
} ]
@@ -686,7 +686,7 @@
"type": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "422549004",
"display": "Patient-related Identification code (observable entity)"
} ]
@@ -734,7 +734,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "370159000",
"display": "Country of Birth"
} ]
@@ -747,7 +747,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "399423000",
"display": "Date of Admission"
} ]
@@ -763,7 +763,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "LA3-6",
"display": "Female"
} ]
@@ -773,7 +773,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "281053000",
"display": "Sex at Birth"
} ]
@@ -785,7 +785,7 @@
"type": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "422549004",
"display": "Patient-related Identification code (observable entity)"
} ]
@@ -824,7 +824,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "399423000",
"display": "Date of Admission"
} ]
@@ -840,7 +840,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "LA3-6",
"display": "Female"
} ]
@@ -850,7 +850,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "281053000",
"display": "Sex at Birth"
} ]
@@ -862,7 +862,7 @@
"type": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "422549004",
"display": "Patient-related Identification code (observable entity)"
} ]
@@ -910,7 +910,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "370159000",
"display": "Country of Birth"
} ]
@@ -923,7 +923,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "399423000",
"display": "Date of Admission"
} ]
@@ -939,7 +939,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "LA3-6",
"display": "Female"
} ]
@@ -949,7 +949,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "281053000",
"display": "Sex at Birth"
} ]
@@ -961,7 +961,7 @@
"type": {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "422549004",
"display": "Patient-related Identification code (observable entity)"
} ]
diff --git a/res/evaluation_cohort/fhir/evco_fhir_procedure.json b/res/evaluation_cohort/fhir/evco_fhir_procedure.json
index d477b3d03..b4528d7ad 100644
--- a/res/evaluation_cohort/fhir/evco_fhir_procedure.json
+++ b/res/evaluation_cohort/fhir/evco_fhir_procedure.json
@@ -29,7 +29,7 @@
"code": {
"coding": [ {
"system": "http://hl7.org/fhir/uv/ips/ValueSet/procedures-uv-ips",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "2752008"
} ]
},
@@ -40,7 +40,7 @@
"bodySite": [ {
"coding": [ {
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "112975008"
} ]
} ]
diff --git a/res/evaluation_cohort/fhir/evco_fhir_variant.json b/res/evaluation_cohort/fhir/evco_fhir_variant.json
index d1ccfe64c..acfa4ac8a 100644
--- a/res/evaluation_cohort/fhir/evco_fhir_variant.json
+++ b/res/evaluation_cohort/fhir/evco_fhir_variant.json
@@ -40,7 +40,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "69548-6",
"display": "Genetic variant assessment"
} ]
@@ -52,7 +52,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48004-6",
"display": "DNA change (c.HGVS)"
} ]
@@ -67,7 +67,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "51958-7",
"display": "Transcript reference sequence [ID]"
} ]
@@ -82,7 +82,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48018-6",
"display": "Gene studied [ID]"
} ]
@@ -98,7 +98,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53034-5",
"display": "Allelic state"
} ]
@@ -106,7 +106,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA6706-1",
"display": "(simple) Heterozygous"
} ]
@@ -146,7 +146,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "69548-6",
"display": "Genetic variant assessment"
} ]
@@ -158,7 +158,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48004-6",
"display": "DNA change (c.HGVS)"
} ]
@@ -173,7 +173,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "51958-7",
"display": "Transcript reference sequence [ID]"
} ]
@@ -188,7 +188,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48018-6",
"display": "Gene studied [ID]"
} ]
@@ -204,7 +204,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53034-5",
"display": "Allelic state"
} ]
@@ -212,7 +212,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA6706-1",
"display": "(simple) Heterozygous"
} ]
@@ -252,7 +252,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "69548-6",
"display": "Genetic variant assessment"
} ]
@@ -264,7 +264,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48004-6",
"display": "DNA change (c.HGVS)"
} ]
@@ -279,7 +279,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "51958-7",
"display": "Transcript reference sequence [ID]"
} ]
@@ -294,7 +294,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48018-6",
"display": "Gene studied [ID]"
} ]
@@ -310,7 +310,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53034-5",
"display": "Allelic state"
} ]
@@ -318,7 +318,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA6706-1",
"display": "(simple) Heterozygous"
} ]
@@ -358,7 +358,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "69548-6",
"display": "Genetic variant assessment"
} ]
@@ -370,7 +370,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48004-6",
"display": "DNA change (c.HGVS)"
} ]
@@ -385,7 +385,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "51958-7",
"display": "Transcript reference sequence [ID]"
} ]
@@ -400,7 +400,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48018-6",
"display": "Gene studied [ID]"
} ]
@@ -416,7 +416,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53034-5",
"display": "Allelic state"
} ]
@@ -424,7 +424,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA6706-1",
"display": "(simple) Heterozygous"
} ]
@@ -464,7 +464,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "69548-6",
"display": "Genetic variant assessment"
} ]
@@ -476,7 +476,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48004-6",
"display": "DNA change (c.HGVS)"
} ]
@@ -491,7 +491,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "51958-7",
"display": "Transcript reference sequence [ID]"
} ]
@@ -506,7 +506,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48018-6",
"display": "Gene studied [ID]"
} ]
@@ -522,7 +522,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53034-5",
"display": "Allelic state"
} ]
@@ -530,7 +530,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA6706-1",
"display": "(simple) Heterozygous"
} ]
@@ -570,7 +570,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "69548-6",
"display": "Genetic variant assessment"
} ]
@@ -582,7 +582,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48004-6",
"display": "DNA change (c.HGVS)"
} ]
@@ -597,7 +597,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "51958-7",
"display": "Transcript reference sequence [ID]"
} ]
@@ -612,7 +612,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48018-6",
"display": "Gene studied [ID]"
} ]
@@ -628,7 +628,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53034-5",
"display": "Allelic state"
} ]
@@ -636,7 +636,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA26217-2",
"display": "Compunt Heterozygous"
} ]
@@ -676,7 +676,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "69548-6",
"display": "Genetic variant assessment"
} ]
@@ -688,7 +688,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48004-6",
"display": "DNA change (c.HGVS)"
} ]
@@ -703,7 +703,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "51958-7",
"display": "Transcript reference sequence [ID]"
} ]
@@ -718,7 +718,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48018-6",
"display": "Gene studied [ID]"
} ]
@@ -734,7 +734,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53034-5",
"display": "Allelic state"
} ]
@@ -742,7 +742,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA26217-2",
"display": "Compunt Heterozygous"
} ]
@@ -782,7 +782,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "69548-6",
"display": "Genetic variant assessment"
} ]
@@ -794,7 +794,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48004-6",
"display": "DNA change (c.HGVS)"
} ]
@@ -809,7 +809,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "51958-7",
"display": "Transcript reference sequence [ID]"
} ]
@@ -824,7 +824,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48018-6",
"display": "Gene studied [ID]"
} ]
@@ -840,7 +840,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53034-5",
"display": "Allelic state"
} ]
@@ -848,7 +848,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA26217-2",
"display": "Compunt Heterozygous"
} ]
@@ -888,7 +888,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "69548-6",
"display": "Genetic variant assessment"
} ]
@@ -900,7 +900,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48004-6",
"display": "DNA change (c.HGVS)"
} ]
@@ -915,7 +915,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "51958-7",
"display": "Transcript reference sequence [ID]"
} ]
@@ -930,7 +930,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48018-6",
"display": "Gene studied [ID]"
} ]
@@ -946,7 +946,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53034-5",
"display": "Allelic state"
} ]
@@ -954,7 +954,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA6706-1",
"display": "(simple) Heterozygous"
} ]
@@ -994,7 +994,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "69548-6",
"display": "Genetic variant assessment"
} ]
@@ -1006,7 +1006,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48004-6",
"display": "DNA change (c.HGVS)"
} ]
@@ -1021,7 +1021,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "51958-7",
"display": "Transcript reference sequence [ID]"
} ]
@@ -1036,7 +1036,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48018-6",
"display": "Gene studied [ID]"
} ]
@@ -1052,7 +1052,7 @@
"code": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53034-5",
"display": "Allelic state"
} ]
@@ -1060,7 +1060,7 @@
"valueCodeableConcept": {
"coding": [ {
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA6706-1",
"display": "(simple) Heterozygous"
} ]
diff --git a/res/evaluation_cohort/phenopackets/10.json b/res/evaluation_cohort/phenopackets/10.json
index e16224fbe..e38225c1c 100644
--- a/res/evaluation_cohort/phenopackets/10.json
+++ b/res/evaluation_cohort/phenopackets/10.json
@@ -302,7 +302,7 @@
"id": "mondo",
"name": "Monarch Disease Ontology",
"url": "https://purl.obolibrary.org/obo/MONDO/",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"namespacePrefix": "MONDO",
"iriPrefix": "http://purl.obolibrary.org/obo/MONDO_"
},
@@ -310,7 +310,7 @@
"id": "hpo",
"name": "Human Phenotype Ontology",
"url": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"namespacePrefix": "HPO",
"iriPrefix": "http://purl.obolibrary.org/obo/HP_"
},
@@ -318,7 +318,7 @@
"id": "loinc",
"name": "Logical Observation Identifiers Names and Codes",
"url": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"namespacePrefix": "LOINC",
"iriPrefix": "http://loinc.org"
},
@@ -326,7 +326,7 @@
"id": "uo",
"name": "Units of Measurement Ontology",
"url": "https://www.ontobee.org/ontology/UO",
- "version": "2023-05-25",
+ "version": "2026-01-16",
"namespacePrefix": "UO",
"iriPrefix": "http://purl.obolibrary.org/obo/UO_"
},
@@ -358,7 +358,7 @@
"id": "geno",
"name": "GENO - The Genotype Ontology",
"url": "https://www.genoontology.org/",
- "version": "2023-10-08",
+ "version": "2026-02-02",
"namespacePrefix": "GENO",
"iriPrefix": "http://purl.obolibrary.org/obo/GENO_"
}
diff --git a/res/evaluation_cohort/phenopackets/3.json b/res/evaluation_cohort/phenopackets/3.json
index 8501768d8..f396abd3b 100644
--- a/res/evaluation_cohort/phenopackets/3.json
+++ b/res/evaluation_cohort/phenopackets/3.json
@@ -253,7 +253,7 @@
"id": "mondo",
"name": "Monarch Disease Ontology",
"url": "https://purl.obolibrary.org/obo/MONDO/",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"namespacePrefix": "MONDO",
"iriPrefix": "http://purl.obolibrary.org/obo/MONDO_"
},
@@ -261,7 +261,7 @@
"id": "hpo",
"name": "Human Phenotype Ontology",
"url": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"namespacePrefix": "HPO",
"iriPrefix": "http://purl.obolibrary.org/obo/HP_"
},
@@ -269,7 +269,7 @@
"id": "loinc",
"name": "Logical Observation Identifiers Names and Codes",
"url": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"namespacePrefix": "LOINC",
"iriPrefix": "http://loinc.org"
},
@@ -277,7 +277,7 @@
"id": "uo",
"name": "Units of Measurement Ontology",
"url": "https://www.ontobee.org/ontology/UO",
- "version": "2023-05-25",
+ "version": "2026-01-16",
"namespacePrefix": "UO",
"iriPrefix": "http://purl.obolibrary.org/obo/UO_"
},
@@ -309,7 +309,7 @@
"id": "geno",
"name": "GENO - The Genotype Ontology",
"url": "https://www.genoontology.org/",
- "version": "2023-10-08",
+ "version": "2026-02-02",
"namespacePrefix": "GENO",
"iriPrefix": "http://purl.obolibrary.org/obo/GENO_"
}
diff --git a/res/evaluation_cohort/phenopackets/4.json b/res/evaluation_cohort/phenopackets/4.json
index da3cb98f9..39e6d6c0b 100644
--- a/res/evaluation_cohort/phenopackets/4.json
+++ b/res/evaluation_cohort/phenopackets/4.json
@@ -200,7 +200,7 @@
"id": "mondo",
"name": "Monarch Disease Ontology",
"url": "https://purl.obolibrary.org/obo/MONDO/",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"namespacePrefix": "MONDO",
"iriPrefix": "http://purl.obolibrary.org/obo/MONDO_"
},
@@ -208,7 +208,7 @@
"id": "hpo",
"name": "Human Phenotype Ontology",
"url": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"namespacePrefix": "HPO",
"iriPrefix": "http://purl.obolibrary.org/obo/HP_"
},
@@ -216,7 +216,7 @@
"id": "loinc",
"name": "Logical Observation Identifiers Names and Codes",
"url": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"namespacePrefix": "LOINC",
"iriPrefix": "http://loinc.org"
},
@@ -224,7 +224,7 @@
"id": "uo",
"name": "Units of Measurement Ontology",
"url": "https://www.ontobee.org/ontology/UO",
- "version": "2023-05-25",
+ "version": "2026-01-16",
"namespacePrefix": "UO",
"iriPrefix": "http://purl.obolibrary.org/obo/UO_"
},
@@ -256,7 +256,7 @@
"id": "geno",
"name": "GENO - The Genotype Ontology",
"url": "https://www.genoontology.org/",
- "version": "2023-10-08",
+ "version": "2026-02-02",
"namespacePrefix": "GENO",
"iriPrefix": "http://purl.obolibrary.org/obo/GENO_"
}
diff --git a/res/evaluation_cohort/phenopackets/5.json b/res/evaluation_cohort/phenopackets/5.json
index 0c8d9e534..14df91cef 100644
--- a/res/evaluation_cohort/phenopackets/5.json
+++ b/res/evaluation_cohort/phenopackets/5.json
@@ -307,7 +307,7 @@
"id": "mondo",
"name": "Monarch Disease Ontology",
"url": "https://purl.obolibrary.org/obo/MONDO/",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"namespacePrefix": "MONDO",
"iriPrefix": "http://purl.obolibrary.org/obo/MONDO_"
},
@@ -315,7 +315,7 @@
"id": "hpo",
"name": "Human Phenotype Ontology",
"url": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"namespacePrefix": "HPO",
"iriPrefix": "http://purl.obolibrary.org/obo/HP_"
},
@@ -323,7 +323,7 @@
"id": "loinc",
"name": "Logical Observation Identifiers Names and Codes",
"url": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"namespacePrefix": "LOINC",
"iriPrefix": "http://loinc.org"
},
@@ -331,7 +331,7 @@
"id": "uo",
"name": "Units of Measurement Ontology",
"url": "https://www.ontobee.org/ontology/UO",
- "version": "2023-05-25",
+ "version": "2026-01-16",
"namespacePrefix": "UO",
"iriPrefix": "http://purl.obolibrary.org/obo/UO_"
},
@@ -363,7 +363,7 @@
"id": "geno",
"name": "GENO - The Genotype Ontology",
"url": "https://www.genoontology.org/",
- "version": "2023-10-08",
+ "version": "2026-02-02",
"namespacePrefix": "GENO",
"iriPrefix": "http://purl.obolibrary.org/obo/GENO_"
}
diff --git a/res/evaluation_cohort/phenopackets/6.json b/res/evaluation_cohort/phenopackets/6.json
index ce6fc37dc..03ab38ab3 100644
--- a/res/evaluation_cohort/phenopackets/6.json
+++ b/res/evaluation_cohort/phenopackets/6.json
@@ -195,7 +195,7 @@
"id": "mondo",
"name": "Monarch Disease Ontology",
"url": "https://purl.obolibrary.org/obo/MONDO/",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"namespacePrefix": "MONDO",
"iriPrefix": "http://purl.obolibrary.org/obo/MONDO_"
},
@@ -203,7 +203,7 @@
"id": "hpo",
"name": "Human Phenotype Ontology",
"url": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"namespacePrefix": "HPO",
"iriPrefix": "http://purl.obolibrary.org/obo/HP_"
},
@@ -211,7 +211,7 @@
"id": "loinc",
"name": "Logical Observation Identifiers Names and Codes",
"url": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"namespacePrefix": "LOINC",
"iriPrefix": "http://loinc.org"
},
@@ -219,7 +219,7 @@
"id": "uo",
"name": "Units of Measurement Ontology",
"url": "https://www.ontobee.org/ontology/UO",
- "version": "2023-05-25",
+ "version": "2026-01-16",
"namespacePrefix": "UO",
"iriPrefix": "http://purl.obolibrary.org/obo/UO_"
},
@@ -251,7 +251,7 @@
"id": "geno",
"name": "GENO - The Genotype Ontology",
"url": "https://www.genoontology.org/",
- "version": "2023-10-08",
+ "version": "2026-02-02",
"namespacePrefix": "GENO",
"iriPrefix": "http://purl.obolibrary.org/obo/GENO_"
}
diff --git a/res/evaluation_cohort/phenopackets/7.json b/res/evaluation_cohort/phenopackets/7.json
index 833945483..0dca29133 100644
--- a/res/evaluation_cohort/phenopackets/7.json
+++ b/res/evaluation_cohort/phenopackets/7.json
@@ -215,7 +215,7 @@
"id": "mondo",
"name": "Monarch Disease Ontology",
"url": "https://purl.obolibrary.org/obo/MONDO/",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"namespacePrefix": "MONDO",
"iriPrefix": "http://purl.obolibrary.org/obo/MONDO_"
},
@@ -223,7 +223,7 @@
"id": "hpo",
"name": "Human Phenotype Ontology",
"url": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"namespacePrefix": "HPO",
"iriPrefix": "http://purl.obolibrary.org/obo/HP_"
},
@@ -231,7 +231,7 @@
"id": "loinc",
"name": "Logical Observation Identifiers Names and Codes",
"url": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"namespacePrefix": "LOINC",
"iriPrefix": "http://loinc.org"
},
@@ -239,7 +239,7 @@
"id": "uo",
"name": "Units of Measurement Ontology",
"url": "https://www.ontobee.org/ontology/UO",
- "version": "2023-05-25",
+ "version": "2026-01-16",
"namespacePrefix": "UO",
"iriPrefix": "http://purl.obolibrary.org/obo/UO_"
},
@@ -271,7 +271,7 @@
"id": "geno",
"name": "GENO - The Genotype Ontology",
"url": "https://www.genoontology.org/",
- "version": "2023-10-08",
+ "version": "2026-02-02",
"namespacePrefix": "GENO",
"iriPrefix": "http://purl.obolibrary.org/obo/GENO_"
}
diff --git a/res/evaluation_cohort/phenopackets/8.json b/res/evaluation_cohort/phenopackets/8.json
index b8bb01ff1..2a3690986 100644
--- a/res/evaluation_cohort/phenopackets/8.json
+++ b/res/evaluation_cohort/phenopackets/8.json
@@ -253,7 +253,7 @@
"id": "mondo",
"name": "Monarch Disease Ontology",
"url": "https://purl.obolibrary.org/obo/MONDO/",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"namespacePrefix": "MONDO",
"iriPrefix": "http://purl.obolibrary.org/obo/MONDO_"
},
@@ -261,7 +261,7 @@
"id": "hpo",
"name": "Human Phenotype Ontology",
"url": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"namespacePrefix": "HPO",
"iriPrefix": "http://purl.obolibrary.org/obo/HP_"
},
@@ -269,7 +269,7 @@
"id": "loinc",
"name": "Logical Observation Identifiers Names and Codes",
"url": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"namespacePrefix": "LOINC",
"iriPrefix": "http://loinc.org"
},
@@ -277,7 +277,7 @@
"id": "uo",
"name": "Units of Measurement Ontology",
"url": "https://www.ontobee.org/ontology/UO",
- "version": "2023-05-25",
+ "version": "2026-01-16",
"namespacePrefix": "UO",
"iriPrefix": "http://purl.obolibrary.org/obo/UO_"
},
@@ -309,7 +309,7 @@
"id": "geno",
"name": "GENO - The Genotype Ontology",
"url": "https://www.genoontology.org/",
- "version": "2023-10-08",
+ "version": "2026-02-02",
"namespacePrefix": "GENO",
"iriPrefix": "http://purl.obolibrary.org/obo/GENO_"
}
diff --git a/res/evaluation_cohort/phenopackets/9.json b/res/evaluation_cohort/phenopackets/9.json
index f2d363ecf..cd598a799 100644
--- a/res/evaluation_cohort/phenopackets/9.json
+++ b/res/evaluation_cohort/phenopackets/9.json
@@ -216,7 +216,7 @@
"id": "mondo",
"name": "Monarch Disease Ontology",
"url": "https://purl.obolibrary.org/obo/MONDO/",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"namespacePrefix": "MONDO",
"iriPrefix": "http://purl.obolibrary.org/obo/MONDO_"
},
@@ -224,7 +224,7 @@
"id": "hpo",
"name": "Human Phenotype Ontology",
"url": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"namespacePrefix": "HPO",
"iriPrefix": "http://purl.obolibrary.org/obo/HP_"
},
@@ -232,7 +232,7 @@
"id": "loinc",
"name": "Logical Observation Identifiers Names and Codes",
"url": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"namespacePrefix": "LOINC",
"iriPrefix": "http://loinc.org"
},
@@ -240,7 +240,7 @@
"id": "uo",
"name": "Units of Measurement Ontology",
"url": "https://www.ontobee.org/ontology/UO",
- "version": "2023-05-25",
+ "version": "2026-01-16",
"namespacePrefix": "UO",
"iriPrefix": "http://purl.obolibrary.org/obo/UO_"
},
@@ -272,7 +272,7 @@
"id": "geno",
"name": "GENO - The Genotype Ontology",
"url": "https://www.genoontology.org/",
- "version": "2023-10-08",
+ "version": "2026-02-02",
"namespacePrefix": "GENO",
"iriPrefix": "http://purl.obolibrary.org/obo/GENO_"
}
diff --git a/res/evaluation_cohort/redcap/2025-06-03.code-search b/res/evaluation_cohort/redcap/2025-06-03.code-search
new file mode 100644
index 000000000..66f266e2a
--- /dev/null
+++ b/res/evaluation_cohort/redcap/2025-06-03.code-search
@@ -0,0 +1,170 @@
+# Query: 2025-06-03
+# ContextLines: 1
+
+35 results - 26 files
+
+res/evaluation_cohort/fhir/evco_fhir_diagnostic_implication.json:
+ 80 "system": "http://purl.obolibrary.org/obo/mondo.owl",
+ 81: "version": "2025-06-03",
+ 82 "code": "0007843"
+
+ 158 "system": "http://purl.obolibrary.org/obo/mondo.owl",
+ 159: "version": "2025-06-03",
+ 160 "code": "0007843"
+
+ 236 "system": "http://purl.obolibrary.org/obo/mondo.owl",
+ 237: "version": "2025-06-03",
+ 238 "code": "0007843"
+
+ 314 "system": "http://purl.obolibrary.org/obo/mondo.owl",
+ 315: "version": "2025-06-03",
+ 316 "code": "0007843"
+
+ 392 "system": "http://purl.obolibrary.org/obo/mondo.owl",
+ 393: "version": "2025-06-03",
+ 394 "code": "0007843"
+
+ 470 "system": "http://purl.obolibrary.org/obo/mondo.owl",
+ 471: "version": "2025-06-03",
+ 472 "code": "0007843"
+
+ 548 "system": "http://purl.obolibrary.org/obo/mondo.owl",
+ 549: "version": "2025-06-03",
+ 550 "code": "0007843"
+
+ 626 "system": "http://purl.obolibrary.org/obo/mondo.owl",
+ 627: "version": "2025-06-03",
+ 628 "code": "0007843"
+
+ 704 "system": "http://purl.obolibrary.org/obo/mondo.owl",
+ 705: "version": "2025-06-03",
+ 706 "code": "0007843"
+
+ 782 "system": "http://purl.obolibrary.org/obo/mondo.owl",
+ 783: "version": "2025-06-03",
+ 784 "code": "0007843"
+
+res/evaluation_cohort/fhir/evco_fhir_family_member_history.json:
+ 77 "system": "http://purl.obolibrary.org/obo/mondo.owl",
+ 78: "version": "2025-06-03",
+ 79 "code": "MONDO:0007843"
+
+res/evaluation_cohort/phenopackets/3.json:
+ 255 "url": "https://purl.obolibrary.org/obo/MONDO/",
+ 256: "version": "2025-06-03",
+ 257 "namespacePrefix": "MONDO",
+
+res/evaluation_cohort/phenopackets/4.json:
+ 202 "url": "https://purl.obolibrary.org/obo/MONDO/",
+ 203: "version": "2025-06-03",
+ 204 "namespacePrefix": "MONDO",
+
+res/evaluation_cohort/phenopackets/5.json:
+ 309 "url": "https://purl.obolibrary.org/obo/MONDO/",
+ 310: "version": "2025-06-03",
+ 311 "namespacePrefix": "MONDO",
+
+res/evaluation_cohort/phenopackets/6.json:
+ 197 "url": "https://purl.obolibrary.org/obo/MONDO/",
+ 198: "version": "2025-06-03",
+ 199 "namespacePrefix": "MONDO",
+
+res/evaluation_cohort/phenopackets/7.json:
+ 217 "url": "https://purl.obolibrary.org/obo/MONDO/",
+ 218: "version": "2025-06-03",
+ 219 "namespacePrefix": "MONDO",
+
+res/evaluation_cohort/phenopackets/8.json:
+ 255 "url": "https://purl.obolibrary.org/obo/MONDO/",
+ 256: "version": "2025-06-03",
+ 257 "namespacePrefix": "MONDO",
+
+res/evaluation_cohort/phenopackets/9.json:
+ 218 "url": "https://purl.obolibrary.org/obo/MONDO/",
+ 219: "version": "2025-06-03",
+ 220 "namespacePrefix": "MONDO",
+
+res/evaluation_cohort/phenopackets/10.json:
+ 304 "url": "https://purl.obolibrary.org/obo/MONDO/",
+ 305: "version": "2025-06-03",
+ 306 "namespacePrefix": "MONDO",
+
+src/fsh/input/fsh/Bundle-rarelink-example.json:
+ 222 "system": "http://purl.obolibrary.org/obo/mondo.owl",
+ 223: "version": "2025-06-03",
+ 224 "code": "0007843"
+
+src/rarelink/rarelink_cdm/python_datamodel/rarelink_2_personal_information.py:
+ 289 description="Monarch Disease Ontology",
+ 290: code_set_version="2025-06-03",
+ 291 )
+
+src/rarelink/rarelink_cdm/python_datamodel/rarelink_3_patient_status.py:
+ 252 description="Monarch Disease Ontology",
+ 253: code_set_version="2025-06-03",
+ 254 )
+
+src/rarelink/rarelink_cdm/python_datamodel/rarelink_4_care_pathway.py:
+ 249 description="Monarch Disease Ontology",
+ 250: code_set_version="2025-06-03",
+ 251 )
+
+src/rarelink/rarelink_cdm/python_datamodel/rarelink_5_diseases.py:
+ 404 description="Monarch Disease Ontology",
+ 405: code_set_version="2025-06-03",
+ 406 )
+
+src/rarelink/rarelink_cdm/python_datamodel/rarelink_6_1_genetic_findings.py:
+ 710 description="Monarch Disease Ontology",
+ 711: code_set_version="2025-06-03",
+ 712 )
+
+src/rarelink/rarelink_cdm/python_datamodel/rarelink_6_4_family_history.py:
+ 433 description="Monarch Disease Ontology",
+ 434: code_set_version="2025-06-03",
+ 435 )
+
+src/rarelink/rarelink_cdm/python_datamodel/rarelink_7_consent.py:
+ 247 description="Monarch Disease Ontology",
+ 248: code_set_version="2025-06-03",
+ 249 )
+
+src/rarelink/rarelink_cdm/python_datamodel/rarelink_cdm.py:
+ 930 description="Monarch Disease Ontology",
+ 931: code_set_version="2025-06-03",
+ 932 )
+
+src/rarelink/rarelink_cdm/python_datamodel/rarelink_repeated_elements.py:
+ 709 description="Monarch Disease Ontology",
+ 710: code_set_version="2025-06-03",
+ 711 )
+
+src/rarelink/tofhir/mappings/familymemberhistory.familyhistory.json:
+ 96 "system": "{{? iif(loinc_75315_2.empty().not(), 'http://purl.obolibrary.org/obo/mondo.owl')}}",
+ 97: "version": "{{? iif(loinc_75315_2.empty().not(),'2025-06-03')}}",
+ 98 "code": "{{? loinc_75315_2}}"
+
+src/rarelink/tofhir/mappings/genomicreporting.genetic_findings.json:
+ 446 "system": "{{? iif(snomedct_106221001_mondo.empty().not(), 'http://purl.obolibrary.org/obo/mondo.owl')}}",
+ 447: "version": "{{? iif(snomedct_106221001_mondo.empty().not(), '2025-06-03')}}"
+ 448 }
+
+src/rarelink/tofhir/mappings/ips.condition.json:
+ 42 "code": "{{? iif(snomedct_64572001_mondo.empty().not(), snomedct_64572001_mondo.substring(6))}}",
+ 43: "version": "{{? iif(snomedct_64572001_mondo.empty().not(), '2025-06-03')}}"
+ 44 },
+
+tests/phenopackets/test_data/101.json:
+ 455 "url": "https://purl.obolibrary.org/obo/MONDO/",
+ 456: "version": "2025-06-03",
+ 457 "namespace_prefix": "MONDO",
+
+tests/phenopackets/test_data/102.json:
+ 248 "url": "https://purl.obolibrary.org/obo/MONDO/",
+ 249: "version": "2025-06-03",
+ 250 "namespacePrefix": "MONDO",
+
+tests/phenopackets/test_data/103.json:
+ 385 "url": "https://purl.obolibrary.org/obo/MONDO/",
+ 386: "version": "2025-06-03",
+ 387 "namespacePrefix": "MONDO",
diff --git a/res/validation/validator.ipynb b/res/validation/validator.ipynb
index 2fc1616db..0546f5e1a 100644
--- a/res/validation/validator.ipynb
+++ b/res/validation/validator.ipynb
@@ -51350,7 +51350,7 @@
" \"id\": \"participantrequired\",\n",
" \"meta\": {\n",
" \"versionId\": \"1\",\n",
- " \"lastUpdated\": \"2025-05-08T23:40:2LNC2788+11:00\",\n",
+ " \"lastUpdated\": \"2025-05-08T23:40:2v2818+11:00\",\n",
" \"source\": \"#TcjkY57nGwDXvXgk\"\n",
" },\n",
" \"extension\": [ {\n",
@@ -834430,7 +834430,7 @@
" \"id\": \"integer\",\n",
" \"meta\": {\n",
" \"versionId\": \"1\",\n",
- " \"lastUpdated\": \"2025-05-08T23:43:2LNC2789+11:00\",\n",
+ " \"lastUpdated\": \"2025-05-08T23:43:2v2819+11:00\",\n",
" \"source\": \"#rETsIT84Bn51S21D\"\n",
" },\n",
" \"extension\": [ {\n",
@@ -1184960,7 +1184960,7 @@
" \"id\": \"valueset-deprecated\",\n",
" \"meta\": {\n",
" \"versionId\": \"1\",\n",
- " \"lastUpdated\": \"2025-05-08T12:44:2LNC2787+00:00\",\n",
+ " \"lastUpdated\": \"2025-05-08T12:44:2v2817+00:00\",\n",
" \"source\": \"#PAAw2Cc1leprGfqK\"\n",
" },\n",
" \"extension\": [ {\n",
@@ -1348645,7 +1348645,7 @@
" \"id\": \"restful-capability-mode\",\n",
" \"meta\": {\n",
" \"versionId\": \"1\",\n",
- " \"lastUpdated\": \"2025-05-08T23:45:1LNC2786+11:00\",\n",
+ " \"lastUpdated\": \"2025-05-08T23:45:1v2816+11:00\",\n",
" \"source\": \"#P4TAWJx0Kg6aJ7cP\",\n",
" \"profile\": [ \"http://hl7.org/fhir/StructureDefinition/shareablevalueset\" ]\n",
" },\n",
@@ -1405341,7 +1405341,7 @@
" \"id\": \"v2-0924\",\n",
" \"meta\": {\n",
" \"versionId\": \"1\",\n",
- " \"lastUpdated\": \"2025-05-08T12:45:4LNC2783+00:00\",\n",
+ " \"lastUpdated\": \"2025-05-08T12:45:4v2813+00:00\",\n",
" \"source\": \"#lLwrEoYYnaOatzrP\",\n",
" \"profile\": [ \"http://hl7.org/fhir/StructureDefinition/shareablevalueset\" ]\n",
" },\n",
diff --git a/src/fsh/input/fsh/Bundle-rarelink-example.json b/src/fsh/input/fsh/Bundle-rarelink-example.json
index a78c5866e..0c09c00f3 100644
--- a/src/fsh/input/fsh/Bundle-rarelink-example.json
+++ b/src/fsh/input/fsh/Bundle-rarelink-example.json
@@ -40,7 +40,7 @@
"coding": [
{
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "370159000",
"display": "Country of Birth"
}
@@ -58,7 +58,7 @@
"coding": [
{
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "399423000",
"display": "Date of Admission"
}
@@ -80,7 +80,7 @@
"coding": [
{
"system": "http://loinc.org",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "LA3-6",
"display": "Female"
}
@@ -93,7 +93,7 @@
"coding": [
{
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "281053000",
"display": "Sex at Birth"
}
@@ -110,7 +110,7 @@
"coding": [
{
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "422549004",
"display": "Patient-related Identification code (observable entity)"
}
@@ -154,7 +154,7 @@
"coding": [
{
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "105727008",
"display": "Age Category"
}
@@ -168,7 +168,7 @@
"coding": [
{
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "263659003",
"display": "Adolescence"
}
@@ -220,7 +220,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/mondo.owl",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"code": "0007843"
}
]
@@ -277,7 +277,7 @@
"coding": [
{
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "69548-6",
"display": "Genetic variant assessment"
}
@@ -292,7 +292,7 @@
"coding": [
{
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48004-6",
"display": "DNA change (c.HGVS)"
}
@@ -312,7 +312,7 @@
"coding": [
{
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "51958-7",
"display": "Transcript reference sequence [ID]"
}
@@ -332,7 +332,7 @@
"coding": [
{
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "48018-6",
"display": "Gene studied [ID]"
}
@@ -353,7 +353,7 @@
"coding": [
{
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "53034-5",
"display": "Allelic state"
}
@@ -363,7 +363,7 @@
"coding": [
{
"system": "http://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA6706-1",
"display": "(simple) Heterozygous"
}
@@ -400,7 +400,7 @@
"coding": [
{
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
}
@@ -414,7 +414,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003577",
"display": "Congenital onset (at birth)"
}
@@ -425,7 +425,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0000400"
}
]
@@ -463,7 +463,7 @@
"coding": [
{
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
}
@@ -476,7 +476,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012826",
"display": "Moderate"
}
@@ -490,7 +490,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
}
@@ -501,7 +501,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0002650"
}
]
@@ -539,7 +539,7 @@
"coding": [
{
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
}
@@ -552,7 +552,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011010",
"display": "Chronic"
}
@@ -566,7 +566,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
}
@@ -577,7 +577,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0034323"
}
]
@@ -615,7 +615,7 @@
"coding": [
{
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
}
@@ -629,7 +629,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0011463",
"display": "Childhood onset (1y-5y)"
}
@@ -640,7 +640,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0001156"
}
]
@@ -678,7 +678,7 @@
"coding": [
{
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
}
@@ -691,7 +691,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0031796",
"display": "Recurrent"
}
@@ -704,7 +704,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012825",
"display": "Mild"
}
@@ -718,7 +718,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003593",
"display": "Infantile onset (28d-1y)"
}
@@ -729,7 +729,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0001252"
}
]
@@ -767,7 +767,7 @@
"coding": [
{
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "410605003",
"display": "Confirmed present"
}
@@ -780,7 +780,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0012828",
"display": "Severe"
}
@@ -794,7 +794,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0003577",
"display": "Congenital onset (at birth)"
}
@@ -805,7 +805,7 @@
"coding": [
{
"system": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"code": "0001627"
}
]
@@ -852,7 +852,7 @@
"coding": [
{
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA12894-4"
}
],
@@ -910,7 +910,7 @@
"coding": [
{
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14695-8"
}
],
@@ -935,7 +935,7 @@
"coding": [
{
"system": "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl",
- "version": "24.01e",
+ "version": "26.02d",
"code": "C14165"
}
]
@@ -979,7 +979,7 @@
"coding": [
{
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LA12894-4"
}
],
@@ -1037,7 +1037,7 @@
"coding": [
{
"system": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"code": "LP14695-8"
}
],
@@ -1062,7 +1062,7 @@
"coding": [
{
"system": "http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl",
- "version": "24.01e",
+ "version": "26.02d",
"code": "C25640"
}
]
diff --git a/src/rarelink/phenopackets/adapter/ontology_routing_adapter.py b/src/rarelink/phenopackets/adapter/ontology_routing_adapter.py
index 3a900b85d..9f31bcaf8 100644
--- a/src/rarelink/phenopackets/adapter/ontology_routing_adapter.py
+++ b/src/rarelink/phenopackets/adapter/ontology_routing_adapter.py
@@ -13,8 +13,6 @@
"ORDO": "diseases",
}
-_PREFIX_RE = re.compile(r"^([A-Za-z][A-Za-z0-9]*)[:_]")
-
_SKIP_FIELDS = frozenset({
"redcap_repeat_instrument",
"redcap_repeat_instance",
diff --git a/src/rarelink/phenopackets/validate.py b/src/rarelink/phenopackets/validate.py
index 7736a1056..f07648b6d 100644
--- a/src/rarelink/phenopackets/validate.py
+++ b/src/rarelink/phenopackets/validate.py
@@ -1,8 +1,8 @@
-# src/rarelink/phenopackets/validate.py
import json
import re
import shutil
import subprocess
+import sys
from pathlib import Path
from typing import List, Tuple, Union
import logging
diff --git a/src/rarelink/phenopackets/write.py b/src/rarelink/phenopackets/write.py
index 58d7a7395..33f824c88 100644
--- a/src/rarelink/phenopackets/write.py
+++ b/src/rarelink/phenopackets/write.py
@@ -1,4 +1,3 @@
-# src/rarelink/phenopackets/write.py
import json
import logging
from pathlib import Path
diff --git a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_2_personal_information.py b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_2_personal_information.py
index 2fc451b30..5dd312175 100644
--- a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_2_personal_information.py
+++ b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_2_personal_information.py
@@ -277,7 +277,7 @@ class SNOMEDCT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="SNOMEDCT",
description="SNOMED CT",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class MONDO(EnumDefinitionImpl):
@@ -287,7 +287,7 @@ class MONDO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="MONDO",
description="Monarch Disease Ontology",
- code_set_version="2025-06-03",
+ code_set_version="2026-03-03",
)
class HP(EnumDefinitionImpl):
@@ -297,7 +297,7 @@ class HP(EnumDefinitionImpl):
_defn = EnumDefinition(
name="HP",
description="Human Phenotype Ontology",
- code_set_version="2025-05-06",
+ code_set_version="2026-02-16",
)
class LOINC(EnumDefinitionImpl):
@@ -307,7 +307,7 @@ class LOINC(EnumDefinitionImpl):
_defn = EnumDefinition(
name="LOINC",
description="Logical Observation Identifiers Names and Codes",
- code_set_version="LNC278",
+ code_set_version="v281",
)
class OMIM(EnumDefinitionImpl):
@@ -337,7 +337,7 @@ class NCIT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="NCIT",
description="NCI Thesaurus OBO Edition",
- code_set_version="24.01e",
+ code_set_version="26.02d",
)
class UO(EnumDefinitionImpl):
@@ -397,7 +397,7 @@ class ICD11(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD11",
description="International Classification of Diseases, Eleventh Revision",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10CM(EnumDefinitionImpl):
@@ -407,7 +407,7 @@ class ICD10CM(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD10CM",
description="International Classification of Diseases, Tenth Revision, Clinical Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10GM(EnumDefinitionImpl):
@@ -417,7 +417,7 @@ class ICD10GM(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD10GM",
description="International Classification of Diseases, Tenth Revision, German Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class SO(EnumDefinitionImpl):
@@ -437,7 +437,7 @@ class GENO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="GENO",
description="GENO - The Genotype Ontology",
- code_set_version="2023-10-08",
+ code_set_version="2026-02-02",
)
class ISO3166(EnumDefinitionImpl):
diff --git a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_3_patient_status.py b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_3_patient_status.py
index 3f06282dd..0f44a95d3 100644
--- a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_3_patient_status.py
+++ b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_3_patient_status.py
@@ -240,7 +240,7 @@ class SNOMEDCT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="SNOMEDCT",
description="SNOMED CT",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class MONDO(EnumDefinitionImpl):
@@ -250,7 +250,7 @@ class MONDO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="MONDO",
description="Monarch Disease Ontology",
- code_set_version="2025-06-03",
+ code_set_version="2026-03-03",
)
class HP(EnumDefinitionImpl):
@@ -260,7 +260,7 @@ class HP(EnumDefinitionImpl):
_defn = EnumDefinition(
name="HP",
description="Human Phenotype Ontology",
- code_set_version="2025-05-06",
+ code_set_version="2026-02-16",
)
class LOINC(EnumDefinitionImpl):
@@ -270,7 +270,7 @@ class LOINC(EnumDefinitionImpl):
_defn = EnumDefinition(
name="LOINC",
description="Logical Observation Identifiers Names and Codes",
- code_set_version="LNC278",
+ code_set_version="v281",
)
class OMIM(EnumDefinitionImpl):
@@ -300,7 +300,7 @@ class NCIT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="NCIT",
description="NCI Thesaurus OBO Edition",
- code_set_version="24.01e",
+ code_set_version="26.02d",
)
class UO(EnumDefinitionImpl):
@@ -360,7 +360,7 @@ class ICD11(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD11",
description="International Classification of Diseases, Eleventh Revision",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10CM(EnumDefinitionImpl): # noqa: F811
@@ -370,7 +370,7 @@ class ICD10CM(EnumDefinitionImpl): # noqa: F811
_defn = EnumDefinition(
name="ICD10CM",
description="International Classification of Diseases, Tenth Revision, Clinical Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10GM(EnumDefinitionImpl):
@@ -380,7 +380,7 @@ class ICD10GM(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD10GM",
description="International Classification of Diseases, Tenth Revision, German Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class SO(EnumDefinitionImpl):
@@ -400,7 +400,7 @@ class GENO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="GENO",
description="GENO - The Genotype Ontology",
- code_set_version="2023-10-08",
+ code_set_version="2026-02-02",
)
class ISO3166(EnumDefinitionImpl):
diff --git a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_4_care_pathway.py b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_4_care_pathway.py
index 8238d425e..07820c1bd 100644
--- a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_4_care_pathway.py
+++ b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_4_care_pathway.py
@@ -237,7 +237,7 @@ class SNOMEDCT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="SNOMEDCT",
description="SNOMED CT",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class MONDO(EnumDefinitionImpl):
@@ -247,7 +247,7 @@ class MONDO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="MONDO",
description="Monarch Disease Ontology",
- code_set_version="2025-06-03",
+ code_set_version="2026-03-03",
)
class HP(EnumDefinitionImpl):
@@ -257,7 +257,7 @@ class HP(EnumDefinitionImpl):
_defn = EnumDefinition(
name="HP",
description="Human Phenotype Ontology",
- code_set_version="2025-05-06",
+ code_set_version="2026-02-16",
)
class LOINC(EnumDefinitionImpl):
@@ -267,7 +267,7 @@ class LOINC(EnumDefinitionImpl):
_defn = EnumDefinition(
name="LOINC",
description="Logical Observation Identifiers Names and Codes",
- code_set_version="LNC278",
+ code_set_version="v281",
)
class OMIM(EnumDefinitionImpl):
@@ -297,7 +297,7 @@ class NCIT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="NCIT",
description="NCI Thesaurus OBO Edition",
- code_set_version="24.01e",
+ code_set_version="26.02d",
)
class UO(EnumDefinitionImpl):
@@ -357,7 +357,7 @@ class ICD11(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD11",
description="International Classification of Diseases, Eleventh Revision",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10CM(EnumDefinitionImpl):
@@ -367,7 +367,7 @@ class ICD10CM(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD10CM",
description="International Classification of Diseases, Tenth Revision, Clinical Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10GM(EnumDefinitionImpl):
@@ -377,7 +377,7 @@ class ICD10GM(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD10GM",
description="International Classification of Diseases, Tenth Revision, German Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class SO(EnumDefinitionImpl):
@@ -397,7 +397,7 @@ class GENO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="GENO",
description="GENO - The Genotype Ontology",
- code_set_version="2023-10-08",
+ code_set_version="2026-02-02",
)
class ISO3166(EnumDefinitionImpl):
diff --git a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_5_diseases.py b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_5_diseases.py
index f68b055d7..821300fb8 100644
--- a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_5_diseases.py
+++ b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_5_diseases.py
@@ -392,7 +392,7 @@ class SNOMEDCT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="SNOMEDCT",
description="SNOMED CT",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class MONDO(EnumDefinitionImpl):
@@ -402,7 +402,7 @@ class MONDO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="MONDO",
description="Monarch Disease Ontology",
- code_set_version="2025-06-03",
+ code_set_version="2026-03-03",
)
class HP(EnumDefinitionImpl):
@@ -412,7 +412,7 @@ class HP(EnumDefinitionImpl):
_defn = EnumDefinition(
name="HP",
description="Human Phenotype Ontology",
- code_set_version="2025-05-06",
+ code_set_version="2026-02-16",
)
class LOINC(EnumDefinitionImpl):
@@ -422,7 +422,7 @@ class LOINC(EnumDefinitionImpl):
_defn = EnumDefinition(
name="LOINC",
description="Logical Observation Identifiers Names and Codes",
- code_set_version="LNC278",
+ code_set_version="v281",
)
class OMIM(EnumDefinitionImpl):
@@ -452,7 +452,7 @@ class NCIT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="NCIT",
description="NCI Thesaurus OBO Edition",
- code_set_version="24.01e",
+ code_set_version="26.02d",
)
class UO(EnumDefinitionImpl):
@@ -512,7 +512,7 @@ class ICD11(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD11",
description="International Classification of Diseases, Eleventh Revision",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10CM(EnumDefinitionImpl):
@@ -522,7 +522,7 @@ class ICD10CM(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD10CM",
description="International Classification of Diseases, Tenth Revision, Clinical Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10GM(EnumDefinitionImpl):
@@ -532,7 +532,7 @@ class ICD10GM(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD10GM",
description="International Classification of Diseases, Tenth Revision, German Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class SO(EnumDefinitionImpl):
@@ -552,7 +552,7 @@ class GENO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="GENO",
description="GENO - The Genotype Ontology",
- code_set_version="2023-10-08",
+ code_set_version="2026-02-02",
)
class ISO3166(EnumDefinitionImpl):
diff --git a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_6_1_genetic_findings.py b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_6_1_genetic_findings.py
index 28fc9a616..c3ec43d11 100644
--- a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_6_1_genetic_findings.py
+++ b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_6_1_genetic_findings.py
@@ -698,7 +698,7 @@ class SNOMEDCT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="SNOMEDCT",
description="SNOMED CT",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class MONDO(EnumDefinitionImpl): # noqa: F811
@@ -708,7 +708,7 @@ class MONDO(EnumDefinitionImpl): # noqa: F811
_defn = EnumDefinition(
name="MONDO",
description="Monarch Disease Ontology",
- code_set_version="2025-06-03",
+ code_set_version="2026-03-03",
)
class HP(EnumDefinitionImpl):
@@ -718,7 +718,7 @@ class HP(EnumDefinitionImpl):
_defn = EnumDefinition(
name="HP",
description="Human Phenotype Ontology",
- code_set_version="2025-05-06",
+ code_set_version="2026-02-16",
)
class LOINC(EnumDefinitionImpl):
@@ -728,7 +728,7 @@ class LOINC(EnumDefinitionImpl):
_defn = EnumDefinition(
name="LOINC",
description="Logical Observation Identifiers Names and Codes",
- code_set_version="LNC278",
+ code_set_version="v281",
)
class OMIM(EnumDefinitionImpl): # noqa: F811
@@ -758,7 +758,7 @@ class NCIT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="NCIT",
description="NCI Thesaurus OBO Edition",
- code_set_version="24.01e",
+ code_set_version="26.02d",
)
class UO(EnumDefinitionImpl):
@@ -818,7 +818,7 @@ class ICD11(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD11",
description="International Classification of Diseases, Eleventh Revision",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10CM(EnumDefinitionImpl):
@@ -828,7 +828,7 @@ class ICD10CM(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD10CM",
description="International Classification of Diseases, Tenth Revision, Clinical Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10GM(EnumDefinitionImpl):
@@ -838,7 +838,7 @@ class ICD10GM(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD10GM",
description="International Classification of Diseases, Tenth Revision, German Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class SO(EnumDefinitionImpl):
@@ -858,7 +858,7 @@ class GENO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="GENO",
description="GENO - The Genotype Ontology",
- code_set_version="2023-10-08",
+ code_set_version="2026-02-02",
)
class ISO3166(EnumDefinitionImpl):
diff --git a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_6_4_family_history.py b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_6_4_family_history.py
index bf7bc611b..ea79300f9 100644
--- a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_6_4_family_history.py
+++ b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_6_4_family_history.py
@@ -421,7 +421,7 @@ class SNOMEDCT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="SNOMEDCT",
description="SNOMED CT",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class MONDO(EnumDefinitionImpl):
@@ -431,7 +431,7 @@ class MONDO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="MONDO",
description="Monarch Disease Ontology",
- code_set_version="2025-06-03",
+ code_set_version="2026-03-03",
)
class HP(EnumDefinitionImpl):
@@ -441,7 +441,7 @@ class HP(EnumDefinitionImpl):
_defn = EnumDefinition(
name="HP",
description="Human Phenotype Ontology",
- code_set_version="2025-05-06",
+ code_set_version="2026-02-16",
)
class LOINC(EnumDefinitionImpl): # noqa: F811
@@ -451,7 +451,7 @@ class LOINC(EnumDefinitionImpl): # noqa: F811
_defn = EnumDefinition(
name="LOINC",
description="Logical Observation Identifiers Names and Codes",
- code_set_version="LNC278",
+ code_set_version="v281",
)
class OMIM(EnumDefinitionImpl):
@@ -481,7 +481,7 @@ class NCIT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="NCIT",
description="NCI Thesaurus OBO Edition",
- code_set_version="24.01e",
+ code_set_version="26.02d",
)
class UO(EnumDefinitionImpl):
@@ -541,7 +541,7 @@ class ICD11(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD11",
description="International Classification of Diseases, Eleventh Revision",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10CM(EnumDefinitionImpl): # noqa: F811
@@ -551,7 +551,7 @@ class ICD10CM(EnumDefinitionImpl): # noqa: F811
_defn = EnumDefinition(
name="ICD10CM",
description="International Classification of Diseases, Tenth Revision, Clinical Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10GM(EnumDefinitionImpl):
@@ -561,7 +561,7 @@ class ICD10GM(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD10GM",
description="International Classification of Diseases, Tenth Revision, German Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class SO(EnumDefinitionImpl):
@@ -581,7 +581,7 @@ class GENO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="GENO",
description="GENO - The Genotype Ontology",
- code_set_version="2023-10-08",
+ code_set_version="2026-02-02",
)
class ISO3166(EnumDefinitionImpl):
diff --git a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_7_consent.py b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_7_consent.py
index 4015f5cf0..cc40df497 100644
--- a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_7_consent.py
+++ b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_7_consent.py
@@ -235,7 +235,7 @@ class SNOMEDCT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="SNOMEDCT",
description="SNOMED CT",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class MONDO(EnumDefinitionImpl):
@@ -245,7 +245,7 @@ class MONDO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="MONDO",
description="Monarch Disease Ontology",
- code_set_version="2025-06-03",
+ code_set_version="2026-03-03",
)
class HP(EnumDefinitionImpl):
@@ -255,7 +255,7 @@ class HP(EnumDefinitionImpl):
_defn = EnumDefinition(
name="HP",
description="Human Phenotype Ontology",
- code_set_version="2025-05-06",
+ code_set_version="2026-02-16",
)
class LOINC(EnumDefinitionImpl):
@@ -265,7 +265,7 @@ class LOINC(EnumDefinitionImpl):
_defn = EnumDefinition(
name="LOINC",
description="Logical Observation Identifiers Names and Codes",
- code_set_version="LNC278",
+ code_set_version="v281",
)
class OMIM(EnumDefinitionImpl):
@@ -295,7 +295,7 @@ class NCIT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="NCIT",
description="NCI Thesaurus OBO Edition",
- code_set_version="24.01e",
+ code_set_version="26.02d",
)
class UO(EnumDefinitionImpl):
@@ -355,7 +355,7 @@ class ICD11(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD11",
description="International Classification of Diseases, Eleventh Revision",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10CM(EnumDefinitionImpl):
@@ -365,7 +365,7 @@ class ICD10CM(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD10CM",
description="International Classification of Diseases, Tenth Revision, Clinical Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10GM(EnumDefinitionImpl):
@@ -375,7 +375,7 @@ class ICD10GM(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD10GM",
description="International Classification of Diseases, Tenth Revision, German Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class SO(EnumDefinitionImpl):
@@ -395,7 +395,7 @@ class GENO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="GENO",
description="GENO - The Genotype Ontology",
- code_set_version="2023-10-08",
+ code_set_version="2026-02-02",
)
class ISO3166(EnumDefinitionImpl):
diff --git a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_cdm.py b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_cdm.py
index 863be7427..cb2df08fd 100755
--- a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_cdm.py
+++ b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_cdm.py
@@ -918,7 +918,7 @@ class SNOMEDCT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="SNOMEDCT",
description="SNOMED CT",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class MONDO(EnumDefinitionImpl):
@@ -928,7 +928,7 @@ class MONDO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="MONDO",
description="Monarch Disease Ontology",
- code_set_version="2025-06-03",
+ code_set_version="2026-03-03",
)
class HP(EnumDefinitionImpl):
@@ -938,7 +938,7 @@ class HP(EnumDefinitionImpl):
_defn = EnumDefinition(
name="HP",
description="Human Phenotype Ontology",
- code_set_version="2025-05-06",
+ code_set_version="2026-02-16",
)
class LOINC(EnumDefinitionImpl):
@@ -948,7 +948,7 @@ class LOINC(EnumDefinitionImpl):
_defn = EnumDefinition(
name="LOINC",
description="Logical Observation Identifiers Names and Codes",
- code_set_version="LNC278",
+ code_set_version="v281",
)
class OMIM(EnumDefinitionImpl):
@@ -978,7 +978,7 @@ class NCIT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="NCIT",
description="NCI Thesaurus OBO Edition",
- code_set_version="24.01e",
+ code_set_version="26.02d",
)
class UO(EnumDefinitionImpl):
@@ -1038,7 +1038,7 @@ class ICD11(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD11",
description="International Classification of Diseases, Eleventh Revision",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10CM(EnumDefinitionImpl):
@@ -1048,7 +1048,7 @@ class ICD10CM(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD10CM",
description="International Classification of Diseases, Tenth Revision, Clinical Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10GM(EnumDefinitionImpl):
@@ -1058,7 +1058,7 @@ class ICD10GM(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD10GM",
description="International Classification of Diseases, Tenth Revision, German Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class SO(EnumDefinitionImpl):
@@ -1078,7 +1078,7 @@ class GENO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="GENO",
description="GENO - The Genotype Ontology",
- code_set_version="2023-10-08",
+ code_set_version="2026-02-02",
)
class ISO3166(EnumDefinitionImpl):
diff --git a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_code_systems.py b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_code_systems.py
index d97684d1a..f135ea184 100755
--- a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_code_systems.py
+++ b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_code_systems.py
@@ -193,7 +193,7 @@ class NCIT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="NCIT",
description="NCI Thesaurus OBO Edition",
- code_set_version="24.01e",
+ code_set_version="26.02d",
)
class UO(EnumDefinitionImpl):
@@ -253,7 +253,7 @@ class ICD11(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD11",
description="International Classification of Diseases, Eleventh Revision",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10CM(EnumDefinitionImpl):
diff --git a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_repeated_elements.py b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_repeated_elements.py
index 13b01aec0..bb13b9d78 100755
--- a/src/rarelink/rarelink_cdm/python_datamodel/rarelink_repeated_elements.py
+++ b/src/rarelink/rarelink_cdm/python_datamodel/rarelink_repeated_elements.py
@@ -697,7 +697,7 @@ class SNOMEDCT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="SNOMEDCT",
description="SNOMED CT",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class MONDO(EnumDefinitionImpl):
@@ -707,7 +707,7 @@ class MONDO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="MONDO",
description="Monarch Disease Ontology",
- code_set_version="2025-06-03",
+ code_set_version="2026-03-03",
)
class HP(EnumDefinitionImpl):
@@ -717,7 +717,7 @@ class HP(EnumDefinitionImpl):
_defn = EnumDefinition(
name="HP",
description="Human Phenotype Ontology",
- code_set_version="2025-05-06",
+ code_set_version="2026-02-16",
)
class LOINC(EnumDefinitionImpl):
@@ -727,7 +727,7 @@ class LOINC(EnumDefinitionImpl):
_defn = EnumDefinition(
name="LOINC",
description="Logical Observation Identifiers Names and Codes",
- code_set_version="LNC278",
+ code_set_version="v281",
)
class OMIM(EnumDefinitionImpl):
@@ -757,7 +757,7 @@ class NCIT(EnumDefinitionImpl):
_defn = EnumDefinition(
name="NCIT",
description="NCI Thesaurus OBO Edition",
- code_set_version="24.01e",
+ code_set_version="26.02d",
)
class UO(EnumDefinitionImpl):
@@ -817,7 +817,7 @@ class ICD11(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD11",
description="International Classification of Diseases, Eleventh Revision",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10CM(EnumDefinitionImpl):
@@ -827,7 +827,7 @@ class ICD10CM(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD10CM",
description="International Classification of Diseases, Tenth Revision, Clinical Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class ICD10GM(EnumDefinitionImpl):
@@ -837,7 +837,7 @@ class ICD10GM(EnumDefinitionImpl):
_defn = EnumDefinition(
name="ICD10GM",
description="International Classification of Diseases, Tenth Revision, German Modification",
- code_set_version="SNOMEDCT_US_2024_09_01",
+ code_set_version="2025AB",
)
class SO(EnumDefinitionImpl):
@@ -857,7 +857,7 @@ class GENO(EnumDefinitionImpl):
_defn = EnumDefinition(
name="GENO",
description="GENO - The Genotype Ontology",
- code_set_version="2023-10-08",
+ code_set_version="2026-02-02",
)
class ISO3166(EnumDefinitionImpl):
diff --git a/src/rarelink/rarelink_cdm/rarelink_cdm_datadictionary - v2_0_6.csv b/src/rarelink/rarelink_cdm/rarelink_cdm_datadictionary - v2_0_6.csv
index 6f0ad23f9..f93fb6ca1 100644
--- a/src/rarelink/rarelink_cdm/rarelink_cdm_datadictionary - v2_0_6.csv
+++ b/src/rarelink/rarelink_cdm/rarelink_cdm_datadictionary - v2_0_6.csv
@@ -4,7 +4,7 @@ snomedct_422549004,rarelink_1_formal_criteria,"
RareLink - 2) Personal In
SNOMED:184099003 | Date of Birth |
Choices: n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.birthDate
- GA4GH Phenopacket Schema v2.0 Element: Individual.date_of_birth"
@@ -33,7 +33,7 @@ Choices:
- SNOMED:32570691000036108 | Intersex
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.extension:individual-recordedSexOrGender
- GA4GH Phenopacket Schema v2.0 Element: Individual.sex"
@@ -52,7 +52,7 @@ Choices:
- SNOMED:48930007 | XYY
- SNOMED:74964007 | Other
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.value
- GA4GH Phenopacket Schema v2.0 Element: Individual.karyotypic_sex"
@@ -65,7 +65,7 @@ Choices:
- SNOMED:33791000087105 | Identifies as nonbinary gender
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.extension:individual-genderIdentity
- GA4GH Phenopacket Schema v2.0 Element: Individual.gender"
@@ -73,7 +73,7 @@ snomedct_370159000,rarelink_2_personal_information,,text,2.5 Country of Birth,,T
SNOMED:370159000 | Country of Birth |
Choices: ISO 3166 - 2 or 3 letter country code
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.extension:patient-birthPlace
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -87,7 +87,7 @@ Choices:
- SNOMED:185924006 | Unknown - Opted-out
- SNOMED:261665006 | Unknown - Other Reason
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.deceased.deceasedBoolean or Observation.value
- GA4GH Phenopacket Schema v2.0 Element: Individual.VitalStatus.status"
@@ -95,7 +95,7 @@ snomedct_398299004,rarelink_3_patient_status,,text,3.2 Time of Death,,"If deceas
SNOMED:398299004 | Time of Death |
Choices: n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Patient.deceasedDateTime
- GA4GH Phenopacket Schema v2.0 Element: Individual.VitalStatus.time_of_death"
@@ -103,7 +103,7 @@ snomedct_184305005,rarelink_3_patient_status,,text,3.3 Cause of Death [ICD10CM],
SNOMED:184305005 | Cause of Death |
Choices: n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.value.coding.code
- GA4GH Phenopacket Schema v2.0 Element: Individual.VitalStatus.cause_of_death"
@@ -119,7 +119,7 @@ Choices:
- SNOMED:419099009 | Dead
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.value.coding.code
- GA4GH Phenopacket Schema v2.0 Element: Individual.time_at_last_encounter.ontology_class"
@@ -128,7 +128,7 @@ SNOMED:412726003 | Length of Gestation at Birth [weeks+days] |
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.component:weeks.valueQuantity and Observation.component:days.valueQuantity
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -138,7 +138,7 @@ Choices:
- SNOMED:373066001 | Yes
- SNOMED:373067005 | No
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code (e.g., ORDO:616874 - Rare disorder without a determined diagnosis after full investigation)
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass (e.g., ORDO:616874 - Rare disorder without a determined diagnosis after full investigation)"
@@ -171,7 +171,7 @@ Choices:
- SNOMED:entered-in-error | Entered in Error
- SNOMED:unknown | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Encounter.status
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -188,7 +188,7 @@ Choices:
- SNOMED:261665006 | Unknown
Version(s):
- HL7 FHIR Version 4.0.1
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Encounter.class
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -198,7 +198,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -207,7 +207,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -216,7 +216,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -225,7 +225,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -234,7 +234,7 @@ SNOMED:64572001 | Disease
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Disease.term:OntologyClass "
@@ -248,7 +248,7 @@ Choices:
- HL7FHIR:refuted | Refuted
- HL7FHIR:entered-in-error | Entered in Error
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
- HL7 FHIR Version 4.0.1
Mapping:
- HL7 FHIR IPS: Condition.Extension(RareLink)
@@ -261,7 +261,7 @@ Choices:
- SNOMED:410672004 | Date
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.onsetString or Observation.valueCodeableConcept
- GA4GH Phenopacket Schema v2.0 Element: Disease.onset "
@@ -270,7 +270,7 @@ SNOMED:298059007 | Date of Onset
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.onsetDateTime
- GA4GH Phenopacket Schema v2.0 Element: Disease.onset "
@@ -282,7 +282,7 @@ Choices:
- SNOMED:410672004 | Date
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.valueCodeableConcept
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -291,7 +291,7 @@ SNOMED:432213005 | Date of Diagnosis
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.recordedDate
- GA4GH Phenopacket Schema v2.0 Element: Disease.onset "
@@ -300,7 +300,7 @@ SNOMED:363698007 | Body Site
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.bodySite.coding:snomed-ct
- GA4GH Phenopacket Schema v2.0 Element: Disease.primary_site.OntologyClass "
@@ -314,7 +314,7 @@ Choices:
- HL7FHIR:remission | Remission
- HL7FHIR:resolved | Resolved
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
- HL7 FHIR Version 4.0.1
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.clinicalStatus
@@ -326,7 +326,7 @@ Choices:
- SNOMED:6736007 | Moderate
- SNOMED:255604002 | Mild
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.severity
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -336,7 +336,7 @@ SNOMED:106221001 | Genomic Diagnosis
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: [Suggested] : Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Interpretation.Diagnosis.disease"
@@ -345,7 +345,7 @@ SNOMED:106221001 | Genomic Diagnosis
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Condition.code
- GA4GH Phenopacket Schema v2.0 Element: Interpretation.Diagnosis.disease
@@ -391,14 +391,14 @@ LOINC:LA26398-0 | Sequencing
LOINC:LA26415-2 | MLPA
LOINC:LA46-8 | Other
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.method
- GA4GH Phenopacket Schema v2.0 Element: n/a"
loinc_81304_8_other,rarelink_6_1_genetic_findings,,text,6.1.4 Other Structural Variant Analysis Method [LOINC],BIOPORTAL:LOINC,Please seach for the method in here (Tip: use OLS or LOINC to search for the code and type it in here).,,,,,[loinc_81304_8] = 'loinc_la46-8',,,,,,"Variable:
LOINC:81304-8 | Structural Variant Analysis Method Other
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.method
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -411,7 +411,7 @@ LOINC:LA14030-3 | NCBI Build 36.1 (hg18)
LOINC:LA14031-1 | NCBI Build 35 (hg17)
LOINC:LA26806-2 | GRCh38 (hg38)
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:genomic-ref-seq
- GA4GH Phenopacket Schema v2.0 Element:"
@@ -420,7 +420,7 @@ LOINC:LP7824-8 | Genetic Mutation String
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.component:Variant.valueString
- GA4GH Phenopacket Schema v2.0 Element: [...].VariantInterpretation.VariationDescriptor.Extension"
@@ -430,7 +430,7 @@ LOINC:81290-9 | Genomic DNA Change
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:Variant.valueCode
- GA4GH Phenopacket Schema v2.0 Element: ""[...]VariantInterpretation.VariationDescriptor.Expression [+] [...].MoleculeContext"""
@@ -439,7 +439,7 @@ LOINC:48004-6 | Sequence DNA Change
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:Variant.valueCode
- GA4GH Phenopacket Schema v2.0 Element: [...]VariantInterpretation.VariationDescriptor.Expression [+] [...].MoleculeContext"
@@ -448,7 +448,7 @@ LOINC:48005-3 | Amino Acid Change
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:AminoAcidChange
- GA4GH Phenopacket Schema v2.0 Element: [...]VariantInterpretation.VariationDescriptor.Expression [+] [...].MoleculeContext"
@@ -460,7 +460,7 @@ LOINC:48018-6 | Gene
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0 Variant profile: Observation.component:Gene
- GA4GH Phenopacket Schema v2.0 Element: [...].GenomicInterpretation.GeneDescriptor.value_id"
@@ -475,7 +475,7 @@ LOINC:LA6707-9 | Hemizygous
LOINC:LA6703-8 | Heteroplasmic
LOINC:LA6704-6 | Homoplasmic
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.component:geneticsAllele.State | VS: Allelic State
- GA4GH Phenopacket Schema v2.0 Element: [...].GenomicInterpretation.VariantInterpretation.variationDescriptor.AllelicState"
@@ -490,7 +490,7 @@ LOINC:LA6707-9 | Hemizygous
LOINC:LA6703-8 | Heteroplasmic
LOINC:LA6704-6 | Homoplasmic
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.component:geneticsAllele.State | VS: Allelic State
- GA4GH Phenopacket Schema v2.0 Element: [...].GenomicInterpretation.VariantInterpretation.variationDescriptor.AllelicState"
@@ -506,7 +506,7 @@ LOINC:LA18196-8 | Likely fetal
LOINC:LA18197-6 | Unknown genomic origin
LOINC:LA26807-0 | De novo
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.component:GenomicSourceClass
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -521,7 +521,7 @@ LOINC:LA6688-1 | Insertion/Deletion
LOINC:LA6689-9 | Inversion
LOINC:LA6690-7 | Substitution
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Variant.type
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -536,7 +536,7 @@ LOINC:LA6688-1 | Insertion/Deletion
LOINC:LA6689-9 | Inversion
LOINC:LA6690-7 | Substitution
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Variant.type
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -550,7 +550,7 @@ LOINC:LA26334-5 | Likely benign
LOINC:LA6675-8 | Benign
LOINC:LA4489-6 | Unknown
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.component:Variant.Interpretation
- GA4GH Phenopacket Schema v2.0 Element: Interpretation.AcmgPathogenicityClassification"
@@ -577,7 +577,7 @@ LOINC:LA30204-4 | Supporting evidence benign
LOINC:LA30205-1 | Strong evidence benign
LOINC:LA30206-9 | Stand-alone evidence pathogenic
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR GenomicsReporting 3.0.0: Observation.extension:Variant.Interpretation
- GA4GH Phenopacket Schema v2.0 Elemen: n/a"
@@ -586,7 +586,7 @@ SNOMED:8116006 | Phenotypic Feature
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.Code
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.type"
@@ -597,7 +597,7 @@ Choices:
- SNOMED:723511001 | Refuted
Version(s):
- GA4GH Phenopacket Schema v2.0
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.Status (Rec VS: observation.status)
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.excluded "
@@ -606,7 +606,7 @@ SNOMED:439272007:704321009=363778006 | Determination Date
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.effectiveDateTime
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.onset "
@@ -615,7 +615,7 @@ HPO:0034382 | Resolution Date
Choices:
n/a
Version(s):
-P25-05-06 2025-05-06
+P25-05-06 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.effectiveDateTime
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.resolution"
@@ -633,7 +633,7 @@ Choices:
- HP:0003596 | Middle age adult onset (40y-60y)
- HP:0003584 | Late adult onset (60y+)
Version(s):
-P25-05-06 2025-05-06
+P25-05-06 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.category
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.onset"
@@ -649,7 +649,7 @@ Choices:
- HP:0011011 | Subactue
- HP:0025153 | Transient
Version(s):
-P25-05-06 2025-05-06
+P25-05-06 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.interpretation
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.modifiers"
@@ -662,7 +662,7 @@ Choices:
- HP:0012829 | Profound
- HP:0012828 | Severe
Version(s):
-P25-05-06 2025-05-06
+P25-05-06 2026-02-16
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.interpretation
- GA4GH Phenopacket Schema v2.0 Element: PhenotypicFeature.severity
@@ -764,7 +764,7 @@ Choices:
- 8462_4, Diastolic Blood Pressure [mmHg]
- other, Other
Version(s):
-- LOINC vLNC278
+- LOINC vv281
Mapping:
- HL7 FHIR Expression v4.0.1: Observation.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.assay"
@@ -803,7 +803,7 @@ snomedct_122869004_ncit,rarelink_6_3_measurements,,text,6.3.6A Procedure [NCIT],
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.procedure"
@@ -811,7 +811,7 @@ snomedct_122869004_snomed,rarelink_6_3_measurements,,text,6.3.6B Procedure [SNOM
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.procedure"
@@ -821,7 +821,7 @@ snomedct_122869004,rarelink_6_3_measurements,,text,"6.3.7 Procedure [SNOMEDCT]",
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.procedure"
@@ -829,7 +829,7 @@ snomedct_122869005_maxo,rarelink_6_3_measurements,,text,"6.3.7 Procedure [MAXO]"
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.code
- GA4GH Phenopacket Schema v2.0 Element: Measurement.procedure"
@@ -837,7 +837,7 @@ snomedct_122869004_bdsite,rarelink_6_3_measurements,,text,6.3.7A Body Site [SNOM
Choices:
- n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1 [Suggested]: Procedure.bodySite
- GA4GH Phenopacket Schema v2.0 Element: n/a"
@@ -867,7 +867,7 @@ Choices:
- SNOMED:261665006 | Unknown
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: n/a
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives → 1 Phenopacket per family member) "
@@ -887,7 +887,7 @@ Choices:
- SNOMED:17945006 | Natural grandmother
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: n/a
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives → 1 Phenopacket per family member) "
@@ -899,7 +899,7 @@ Choices:
- SNOMED:261665006 | Unknown
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Family.consanguinous_parents
- GA4GH Phenopacket Schema v2.0 Element: (Family.consanguinous_parents) "
@@ -919,7 +919,7 @@ Choices:
- SNOMED:17945006 | Natural grandmother
- SNOMED:1220561009 | Not recorded
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.relationship.coding (VS: FamilyMember)
- GA4GH Phenopacket Schema v2.0 Element: Family.Pedigree.Person.individual_id "
@@ -944,8 +944,8 @@ Choices:
- SNOMED:32570691000036108 | Intersex
- SNOMED:1220561009 | Not recorded
Version(s):
-- LOINC vLNC278 LNC278
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- LOINC vv281 v281
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.sex (VS: AdministrativeGender)
- GA4GH Phenopacket Schema v2.0 Element: Family.Pedigree.Person.sex "
@@ -954,7 +954,7 @@ LOINC:54141-7 | Family Member Age
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.ageAge
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -963,7 +963,7 @@ LOINC:54124-3 | Family Member Date of Birth
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.bornDate
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -974,7 +974,7 @@ Choices:
- SNOMED:373067005 | No
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.deceased.deceasedBoolean
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -983,7 +983,7 @@ LOINC:54112-8 | Family Member Cause of Death
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.condition.code & FamilyMemberHistory.condition.contributedToDeath
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -992,7 +992,7 @@ LOINC:92662-6 | Family Member Deceased Age
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.deceasedAge
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -1001,7 +1001,7 @@ LOINC:75315-2 | Family Member Disease
Choices:
n/a
Version(s):
-- LOINC vLNC278 LNC278
+- LOINC vv281 v281
Mapping:
- HL7 FHIR Expression v4.0.1: FamilyMemberHistory.condition.code
- GA4GH Phenopacket Schema v2.0 Element: (Family.relatives) "
@@ -1015,7 +1015,7 @@ Choices:
- HL7FHIR:inactive | Inactive
- HL7FHIR:entered-in-error | Entered in Error
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Consent.status
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -1033,7 +1033,7 @@ SNOMED:386318002 | Health Policy Monitoring
Choices:
n/a
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Consent.policy
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -1046,7 +1046,7 @@ Choices:
- SNOMED:261665006 | Unknown
Version(s):
- RareLink Custom Codes Version 2.0
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Consent.scope.coding
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -1059,7 +1059,7 @@ Choices:
- SNOMED:261665006 | Unknown
Version(s):
- RareLink Custom Codes Version 2.0
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: Consent.scope.coding
- GA4GH Phenopacket Schema v2.0 Element: n/a "
@@ -1071,7 +1071,7 @@ Choices:
- SNOMED:373067005 | No
- SNOMED:261665006 | Unknown
Version(s):
-- SNOMED CT SNOMEDCT_US_2024_09_01 SNOMEDCT_US_2024_09_01
+- SNOMED CT 2025AB 2025AB
Mapping:
- HL7 FHIR Expression v4.0.1: n/a
- GA4GH Phenopacket Schema v2.0 Element: n/a "
diff --git a/src/rarelink/rarelink_cdm/schema_definitions/rarelink_2_personal_information.yaml b/src/rarelink/rarelink_cdm/schema_definitions/rarelink_2_personal_information.yaml
index d53287aaa..c67e0c4dc 100755
--- a/src/rarelink/rarelink_cdm/schema_definitions/rarelink_2_personal_information.yaml
+++ b/src/rarelink/rarelink_cdm/schema_definitions/rarelink_2_personal_information.yaml
@@ -59,7 +59,7 @@ enums:
permissible_values:
snomedct_248152002:
description: Female
- meaning: LOINC:76689-9
+ meaning: SNOMEDCT:248152002
snomedct_248153007:
description: Male
meaning: SNOMEDCT:248153007
diff --git a/src/rarelink/rarelink_cdm/schema_definitions/rarelink_6_4_family_history.yaml b/src/rarelink/rarelink_cdm/schema_definitions/rarelink_6_4_family_history.yaml
index 4603d9d60..48fa7afe8 100755
--- a/src/rarelink/rarelink_cdm/schema_definitions/rarelink_6_4_family_history.yaml
+++ b/src/rarelink/rarelink_cdm/schema_definitions/rarelink_6_4_family_history.yaml
@@ -274,7 +274,7 @@ enums:
permissible_values:
snomedct_248152002:
description: Female
- meaning: LOINC:76689-9
+ meaning: SNOMEDCT:248152002
snomedct_248153007:
description: Male
meaning: SNOMEDCT:248153007
diff --git a/src/rarelink/rarelink_cdm/schema_definitions/rarelink_code_systems.yaml b/src/rarelink/rarelink_cdm/schema_definitions/rarelink_code_systems.yaml
index 6df07db58..f4e958f84 100755
--- a/src/rarelink/rarelink_cdm/schema_definitions/rarelink_code_systems.yaml
+++ b/src/rarelink/rarelink_cdm/schema_definitions/rarelink_code_systems.yaml
@@ -40,7 +40,7 @@ enums:
NCIT:
description: NCI Thesaurus OBO Edition
code_set: http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl
- code_set_version: '24.01e'
+ code_set_version: '26.02d'
UO:
description: Units of Measurement Ontology
code_set: https://www.ontobee.org/ontology/UO
@@ -64,7 +64,7 @@ enums:
ICD11:
description: International Classification of Diseases, Eleventh Revision
code_set: https://icd.who.int/en
- code_set_version: 'SNOMEDCT_US_2024_09_01'
+ code_set_version: '2025AB'
ICD10CM:
description: International Classification of Diseases, Tenth Revision, Clinical
Modification
diff --git a/src/rarelink/tofhir/mapping-contexts/4_4_encounter_class.csv b/src/rarelink/tofhir/mapping-contexts/4_4_encounter_class.csv
index b13705d16..57237db7c 100644
--- a/src/rarelink/tofhir/mapping-contexts/4_4_encounter_class.csv
+++ b/src/rarelink/tofhir/mapping-contexts/4_4_encounter_class.csv
@@ -6,4 +6,4 @@
"hl7fhir_vr","Virtual","VR","Virtual","https://hl7.org/fhir/R4/","R4"
"hl7fhir_hh","Home Health","HH","Home Health","https://hl7.org/fhir/R4/","R4"
"rarelink_rdc","RD Specialist Center","RDC","RD Specialist Center","https://github.com/BIH-CEI/RareLink","2.0+"
-"snomedct_261665006","Unknown","261665006","Unknown","http://snomed.info/sct","SNOMEDCT_US_2024_09_01"
\ No newline at end of file
+"snomedct_261665006","Unknown","261665006","Unknown","http://snomed.info/sct","2025AB"
\ No newline at end of file
diff --git a/src/rarelink/tofhir/mapping-contexts/jsons/4_4_encounter_class.json b/src/rarelink/tofhir/mapping-contexts/jsons/4_4_encounter_class.json
index 6fce118f6..b9ff890c3 100755
--- a/src/rarelink/tofhir/mapping-contexts/jsons/4_4_encounter_class.json
+++ b/src/rarelink/tofhir/mapping-contexts/jsons/4_4_encounter_class.json
@@ -64,7 +64,7 @@
"target_code": "261665006",
"target_display": "Unknown",
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01"
+ "version": "2025AB"
}
]
}
\ No newline at end of file
diff --git a/src/rarelink/tofhir/mappings/consent.consent.json b/src/rarelink/tofhir/mappings/consent.consent.json
index 65aa94c3a..41ba0be5d 100755
--- a/src/rarelink/tofhir/mappings/consent.consent.json
+++ b/src/rarelink/tofhir/mappings/consent.consent.json
@@ -81,7 +81,7 @@
"coding": [
{
"system": "{{? iif(rarelink_consent_contact.empty().not(), 'http://snomed.info/sct')}}",
- "version": "{{? iif(rarelink_consent_contact.empty().not(), 'SNOMEDCT_US_2024_09_01')}}",
+ "version": "{{? iif(rarelink_consent_contact.empty().not(), '2025AB')}}",
"code": "{{? mpp:getConcept(%consentContact, rarelink_consent_contact, 'target_code')}}",
"display": "{{? mpp:getConcept(%consentContact, rarelink_consent_contact, 'target_display')}}"
}
diff --git a/src/rarelink/tofhir/mappings/familymemberhistory.familyhistory.json b/src/rarelink/tofhir/mappings/familymemberhistory.familyhistory.json
index 9d286ddb2..fcd9b0598 100644
--- a/src/rarelink/tofhir/mappings/familymemberhistory.familyhistory.json
+++ b/src/rarelink/tofhir/mappings/familymemberhistory.familyhistory.json
@@ -36,7 +36,7 @@
"coding": [
{
"system": "{{'http://snomed.info/sct'}}",
- "version": "{{'SNOMEDCT_US_2024_09_01'}}",
+ "version": "{{'2025AB'}}",
"code": "{{mpp:getConcept(%familyRelationship, snomedct_444018008, 'target_code')}}",
"display": "{{mpp:getConcept(%familyRelationship, snomedct_444018008, 'target_display')}}"
}
@@ -46,7 +46,7 @@
"coding": [
{
"system": "{{? iif(loinc_54123_5.empty().not(),'http://hl7.org/fhir/ValueSet/administrative-gender')}}",
- "version": "{{? iif(loinc_54123_5.empty().not(),'SNOMEDCT_US_2024_09_01')}}",
+ "version": "{{? iif(loinc_54123_5.empty().not(),'2025AB')}}",
"code": "{{? mpp:getConcept(%familySex, loinc_54123_5, 'target_code')}}",
"display": "{{? mpp:getConcept(%familySex, loinc_54123_5, 'target_display')}}"
}
@@ -81,7 +81,7 @@
"coding": [
{
"system": "{{? iif(loinc_54112_8.empty().not(), 'https://www.cdc.gov/nchs/icd/icd10cm.htm')}}",
- "version": "{{? iif(loinc_54112_8.empty().not(), 'SNOMEDCT_US_2024_09_01')}}",
+ "version": "{{? iif(loinc_54112_8.empty().not(), '2025AB')}}",
"code": "{{? loinc_54112_8}}"
}
],
@@ -94,7 +94,7 @@
"coding": [
{
"system": "{{? iif(loinc_75315_2.empty().not(), 'http://purl.obolibrary.org/obo/mondo.owl')}}",
- "version": "{{? iif(loinc_75315_2.empty().not(),'2025-06-03')}}",
+ "version": "{{? iif(loinc_75315_2.empty().not(),'2026-03-03')}}",
"code": "{{? loinc_75315_2}}"
}
],
@@ -111,7 +111,7 @@
"url": "{{? iif(snomedct_64245008.empty().not(), 'https://rarelink.bih-charite.de/fhir/StructureDefinition/propositus')}}",
"valueCoding": {
"system": "{{? iif(snomedct_64245008.empty().not(), 'http://snomed.info/sct')}}",
- "version": "{{? iif(snomedct_64245008.empty().not(), 'SNOMEDCT_US_2024_09_01')}}",
+ "version": "{{? iif(snomedct_64245008.empty().not(), '2025AB')}}",
"code": "{{? iif(snomedct_64245008.empty().not(), '64245008')}}",
"display": "{{? iif(snomedct_64245008.empty().not(), 'Propositus (finding)')}}"
},
@@ -119,7 +119,7 @@
"coding": [
{
"system": "{{? iif(snomedct_64245008.empty().not(), 'http://snomed.info/sct')}}",
- "version": "{{? iif(snomedct_64245008.empty().not(), 'SNOMEDCT_US_2024_09_01')}}",
+ "version": "{{? iif(snomedct_64245008.empty().not(), '2025AB')}}",
"code": "{{? mpp:getConcept(%familyPropositus, snomedct_64245008, 'target_code')}}",
"display": "{{? mpp:getConcept(%familyPropositus, snomedct_64245008, 'target_display')}}"
}
@@ -130,7 +130,7 @@
"url": "{{? iif(snomedct_842009.empty().not(), 'https://rarelink.bih-charite.de/fhir/StructureDefinition/consanguinity')}}",
"valueCoding": {
"system": "{{? iif(snomedct_842009.empty().not(), 'http://snomed.info/sct')}}",
- "version": "{{? iif(snomedct_842009.empty().not(), 'SNOMEDCT_US_2024_09_01')}}",
+ "version": "{{? iif(snomedct_842009.empty().not(), '2025AB')}}",
"code": "{{? iif(snomedct_842009.empty().not(), '842009')}}",
"display": "{{? iif(snomedct_842009.empty().not(), 'Consanguinity (finding)')}}"
},
@@ -138,7 +138,7 @@
"coding": [
{
"system": "{{? iif(snomedct_842009.empty().not(), 'http://snomed.info/sct')}}",
- "version": "{{? iif(snomedct_842009.empty().not(), 'SNOMEDCT_US_2024_09_01')}}",
+ "version": "{{? iif(snomedct_842009.empty().not(), '2025AB')}}",
"code": "{{? mpp:getConcept(%familyConsanguinity, snomedct_842009, 'target_code')}}",
"display": "{{? mpp:getConcept(%familyConsanguinity, snomedct_842009, 'target_display')}}"
}
diff --git a/src/rarelink/tofhir/mappings/genomicreporting.genetic_findings.json b/src/rarelink/tofhir/mappings/genomicreporting.genetic_findings.json
index 9989b5c36..d4a0b3d20 100644
--- a/src/rarelink/tofhir/mappings/genomicreporting.genetic_findings.json
+++ b/src/rarelink/tofhir/mappings/genomicreporting.genetic_findings.json
@@ -30,7 +30,7 @@
{
"code": "{{'69548-6'}}",
"system": "{{'http://loinc.org'}}",
- "version": "{{'LNC278'}}",
+ "version": "{{'v281'}}",
"display": "{{'Genetic variant assessment'}}"
}
]
@@ -42,7 +42,7 @@
"{{?}}": {
"code": "{{? mpp:getConcept(%geneticsMethod, loinc_81304_8, 'target_code')}}",
"system": "{{? iif(loinc_81304_8.empty().not(), 'https://loinc.org/')}}",
- "version": "{{? iif(loinc_81304_8.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_81304_8.empty().not(), 'v281')}}",
"display": "{{? mpp:getConcept(%geneticsMethod, loinc_81304_8, 'target_display')}}"
}
},
@@ -51,7 +51,7 @@
"{{?}}": {
"code": "{{? loinc_81304_8_other}}",
"system": "{{? iif(loinc_81304_8.empty().not(), 'https://loinc.org/')}}",
- "version": "{{? iif(loinc_81304_8.empty().not(), 'LNC278')}}"
+ "version": "{{? iif(loinc_81304_8.empty().not(), 'v281')}}"
}
}
]
@@ -83,7 +83,7 @@
{
"code": "{{? iif(loinc_81290_9.empty().not(), '81290-9')}}",
"system": "{{? iif(loinc_81290_9.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_81290_9.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_81290_9.empty().not(), 'v281')}}",
"display": "{{? iif(loinc_81290_9.empty().not(), 'Genomic DNA change (gHGVS)')}}"
}
]
@@ -104,7 +104,7 @@
{
"code": "{{? iif(loinc_81290_9.empty().not(), '48013-7')}}",
"system": "{{? iif(loinc_81290_9.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_81290_9.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_81290_9.empty().not(), 'v281')}}",
"display": "{{? iif(loinc_81290_9.empty().not(), 'Genomic reference sequence [ID]')}}"
}
]
@@ -125,7 +125,7 @@
{
"code": "{{? iif(loinc_48004_6.empty().not(), '48004-6')}}",
"system": "{{? iif(loinc_48004_6.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_48004_6.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_48004_6.empty().not(), 'v281')}}",
"display": "{{? iif(loinc_48004_6.empty().not(), 'DNA change (c.HGVS)')}}"
}
]
@@ -146,7 +146,7 @@
{
"code": "{{? iif(loinc_48004_6.empty().not(), '51958-7')}}",
"system": "{{? iif(loinc_48004_6.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_48004_6.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_48004_6.empty().not(), 'v281')}}",
"display": "{{? iif(loinc_48004_6.empty().not(), 'Transcript reference sequence [ID]')}}"
}
]
@@ -167,7 +167,7 @@
{
"code": "{{? iif(loinc_48005_3.empty().not(), '48005-3')}}",
"system": "{{? iif(loinc_48005_3.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_48005_3.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_48005_3.empty().not(), 'v281')}}",
"display": "{{? iif(loinc_48005_3.empty().not(), 'Amino acid change (pHGVS)')}}"
}
]
@@ -209,7 +209,7 @@
{
"code": "{{? iif(loinc_62374_4.empty().not(), '62374-4')}}",
"system": "{{? iif(loinc_62374_4.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_62374_4.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_62374_4.empty().not(), 'v281')}}",
"display": "{{? iif(loinc_62374_4.empty().not(), 'Human reference sequence assembly version')}}"
}
]
@@ -219,7 +219,7 @@
{
"code": "{{? mpp:getConcept(%geneticsReferenceGenome, loinc_62374_4, 'target_code')}}",
"system": "{{? iif(loinc_62374_4.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_62374_4.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_62374_4.empty().not(), 'v281')}}",
"display": "{{? mpp:getConcept(%geneticsReferenceGenome, loinc_62374_4, 'target_display')}}"
}
]
@@ -232,7 +232,7 @@
{
"code": "{{? iif(loinc_48018_6.empty().not(), '48018-6')}}",
"system": "{{? iif(loinc_48018_6.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_48018_6.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_48018_6.empty().not(), 'v281')}}",
"display": "{{? iif(loinc_48018_6.empty().not(), 'Gene studied [ID]')}}"
}
]
@@ -254,7 +254,7 @@
{
"code": "{{? iif(loinc_53034_5.empty().not(), '53034-5')}}",
"system": "{{? iif(loinc_53034_5.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_53034_5.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_53034_5.empty().not(), 'v281')}}",
"display": "{{? iif(loinc_53034_5.empty().not(), 'Allelic state')}}"
}
]
@@ -266,7 +266,7 @@
"{{?}}": {
"code": "{{? mpp:getConcept(%geneticsZygosity, loinc_53034_5, 'target_code')}}",
"system": "{{? iif(loinc_53034_5.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_53034_5.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_53034_5.empty().not(), 'v281')}}",
"display": "{{? mpp:getConcept(%geneticsZygosity, loinc_53034_5, 'target_display')}}"
}
},
@@ -275,7 +275,7 @@
"{{?}}": {
"code": "{{? loinc_53034_5_other}}",
"system": "{{? iif(loinc_53034_5_other.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_53034_5_other.empty().not(), 'LNC278')}}"
+ "version": "{{? iif(loinc_53034_5_other.empty().not(), 'v281')}}"
}
}
]
@@ -288,7 +288,7 @@
{
"code": "{{? iif(loinc_48002_0.empty().not(), '48002-0')}}",
"system": "{{? iif(loinc_48002_0.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_48002_0.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_48002_0.empty().not(), 'v281')}}",
"display": "{{? iif(loinc_48002_0.empty().not(), 'Genomic source class [Type]')}}"
}
]
@@ -298,7 +298,7 @@
{
"code": "{{? mpp:getConcept(%geneticsGenomicSourceClass, loinc_48002_0, 'target_code')}}",
"system": "{{? iif(loinc_48002_0.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_48002_0.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_48002_0.empty().not(), 'v281')}}",
"display": "{{? mpp:getConcept(%geneticsGenomicSourceClass, loinc_48002_0, 'target_display')}}"
}
]
@@ -311,7 +311,7 @@
{
"code": "{{? iif(loinc_48019_4.empty().not(), '48019-4')}}",
"system": "{{? iif(loinc_48019_4.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_48019_4.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_48019_4.empty().not(), 'v281')}}",
"display": "{{? iif(loinc_48019_4.empty().not(), 'DNA change type')}}"
}
]
@@ -323,7 +323,7 @@
"{{?}}": {
"code": "{{? mpp:getConcept(%geneticsDNAChangeType, loinc_48019_4, 'target_code')}}",
"system": "{{? iif(loinc_48019_4.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_48019_4.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_48019_4.empty().not(), 'v281')}}",
"display": "{{? mpp:getConcept(%geneticsDNAChangeType, loinc_48019_4, 'target_display')}}"
}
},
@@ -332,7 +332,7 @@
"{{?}}": {
"code": "{{? loinc_48019_4_other}}",
"system": "{{? iif(loinc_48019_4_other.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_48019_4_other.empty().not(), 'LNC278')}}"
+ "version": "{{? iif(loinc_48019_4_other.empty().not(), 'v281')}}"
}
}
]
@@ -386,7 +386,7 @@
{
"code": "{{? iif(loinc_93044_6.empty().not(), '93044-6')}}",
"system": "{{? iif(loinc_93044_6.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_93044_6.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_93044_6.empty().not(), 'v281')}}",
"display": "{{? iif(loinc_93044_6.empty().not(), 'Level of evidence')}}"
}
]
@@ -396,7 +396,7 @@
{
"code": "{{? mpp:getConcept(%geneticsClinicalAnnotation, loinc_93044_6, 'target_code')}}",
"system": "{{? iif(loinc_93044_6.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_93044_6.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_93044_6.empty().not(), 'v281')}}",
"display": "{{? mpp:getConcept(%geneticsClinicalAnnotation, loinc_93044_6, 'target_display')}}"
}
]
@@ -409,7 +409,7 @@
{
"code": "{{? iif(loinc_53037_8.empty().not(), '53037-8')}}",
"system": "{{? iif(loinc_53037_8.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_53037_8.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_53037_8.empty().not(), 'v281')}}",
"display": "{{? iif(loinc_53037_8.empty().not(), 'Genetic variation clinical significance [Imp]')}}"
}
]
@@ -419,7 +419,7 @@
{
"code": "{{? mpp:getConcept(%geneticsClinicalSignifiance, loinc_53037_8, 'target_code')}}",
"system": "{{? iif(loinc_53037_8.empty().not(), 'http://loinc.org')}}",
- "version": "{{? iif(loinc_53037_8.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(loinc_53037_8.empty().not(), 'v281')}}",
"display": "{{? mpp:getConcept(%geneticsClinicalSignifiance, loinc_53037_8, 'target_display')}}"
}
]
@@ -432,7 +432,7 @@
{
"code": "{{'81259-4'}}",
"system": "{{'http://loinc.org'}}",
- "version": "{{'LNC278'}}",
+ "version": "{{'v281'}}",
"display": "{{'Associated phenotype'}}"
}
]
@@ -444,7 +444,7 @@
"{{?}}": {
"code": "{{? snomedct_106221001_mondo.substring(6)}}",
"system": "{{? iif(snomedct_106221001_mondo.empty().not(), 'http://purl.obolibrary.org/obo/mondo.owl')}}",
- "version": "{{? iif(snomedct_106221001_mondo.empty().not(), '2025-06-03')}}"
+ "version": "{{? iif(snomedct_106221001_mondo.empty().not(), '2026-03-03')}}"
}
},
{
diff --git a/src/rarelink/tofhir/mappings/ips.condition.json b/src/rarelink/tofhir/mappings/ips.condition.json
index 43bc064a1..08006823e 100644
--- a/src/rarelink/tofhir/mappings/ips.condition.json
+++ b/src/rarelink/tofhir/mappings/ips.condition.json
@@ -40,7 +40,7 @@
{
"system": "{{? iif(snomedct_64572001_mondo.empty().not(), 'http://purl.obolibrary.org/obo/mondo.owl')}}",
"code": "{{? iif(snomedct_64572001_mondo.empty().not(), snomedct_64572001_mondo.substring(6))}}",
- "version": "{{? iif(snomedct_64572001_mondo.empty().not(), '2025-06-03')}}"
+ "version": "{{? iif(snomedct_64572001_mondo.empty().not(), '2026-03-03')}}"
},
{
"system": "{{? iif(snomedct_64572001_ordo.empty().not(), 'http://www.orpha.net/')}}",
@@ -60,7 +60,7 @@
{
"system": "{{? iif(snomedct_64572001_icd11.empty().not(), 'https://icd.who.int/en')}}",
"code": "{{? iif(snomedct_64572001_icd11.empty().not(), snomedct_64572001_icd11)}}",
- "version": "{{? iif(snomedct_64572001_icd11.empty().not(), 'SNOMEDCT_US_2024_09_01')}}"
+ "version": "{{? iif(snomedct_64572001_icd11.empty().not(), '2025AB')}}"
}
]
},
@@ -80,7 +80,7 @@
"system": "{{? iif(snomedct_246112005.empty().not(), 'http://snomed.info/sct')}}",
"code": "{{? mpp:getConcept(%diseaseSeverity, snomedct_246112005, 'target_code')}}",
"display": "{{? mpp:getConcept(%diseaseSeverity, snomedct_246112005, 'target_display')}}",
- "version": "{{? iif(snomedct_246112005.empty().not(), 'SNOMEDCT_US_2024_09_01')}}"
+ "version": "{{? iif(snomedct_246112005.empty().not(), '2025AB')}}"
}
]
},
@@ -90,7 +90,7 @@
{
"system": "{{? iif(snomedct_363698007.empty().not(), 'http://snomed.info/sct')}}",
"code": "{{? snomedct_363698007}}",
- "version": "{{? iif(snomedct_363698007.empty().not(), 'SNOMEDCT_US_2024_09_01')}}"
+ "version": "{{? iif(snomedct_363698007.empty().not(), '2025AB')}}"
}
]
}
@@ -117,7 +117,7 @@
"system": "{{? iif(snomedct_423493009.empty().not(), 'http://snomed.info/sct')}}",
"code": "{{? mpp:getConcept(%rarelinkAgeAtDiagnosis, snomedct_423493009, 'target_code')}}",
"display": "{{? mpp:getConcept(%rarelinkAgeAtDiagnosis, snomedct_423493009, 'target_display')}}",
- "version": "{{? iif(snomedct_423493009.empty().not(), 'SNOMEDCT_US_2024_09_01')}}"
+ "version": "{{? iif(snomedct_423493009.empty().not(), '2025AB')}}"
}
],
"text": "{{? iif(snomedct_423493009.empty().not(), 'SNOMED:423493009 - Age at Diagnosis')}}"
@@ -132,7 +132,7 @@
"system": "{{? iif(snomedct_424850005.empty().not(), 'http://snomed.info/sct')}}",
"code": "{{? mpp:getConcept(%diseaseAgeAtOnset, snomedct_424850005, 'target_code')}}",
"display": "{{? mpp:getConcept(%diseaseAgeAtOnset, snomedct_424850005, 'target_display')}}",
- "version": "{{? iif(snomedct_424850005.empty().not(), 'SNOMEDCT_US_2024_09_01')}}"
+ "version": "{{? iif(snomedct_424850005.empty().not(), '2025AB')}}"
}
],
"text": "{{? iif(snomedct_424850005.empty().not(), 'SNOMED:424850005 - Age at Onset')}}"
diff --git a/src/rarelink/tofhir/mappings/ips.measurement.laboratory.json b/src/rarelink/tofhir/mappings/ips.measurement.laboratory.json
index 170d46855..7de019ec9 100644
--- a/src/rarelink/tofhir/mappings/ips.measurement.laboratory.json
+++ b/src/rarelink/tofhir/mappings/ips.measurement.laboratory.json
@@ -43,7 +43,7 @@
{
"system": "{{'https://loinc.org'}}",
"code": "{{ncit_c60819}}",
- "version": "{{'LNC278'}}"
+ "version": "{{'v281'}}"
}
],
"text": "{{'Measurements - Assay'}}"
@@ -70,7 +70,7 @@
{
"system": "{{? iif(ncit_c41255.empty().not(), 'http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl')}}",
"code": "{{? ncit_c41255.substring(10)}}",
- "version": "{{? iif(ncit_c41255.empty().not(), '24.01e')}}"
+ "version": "{{? iif(ncit_c41255.empty().not(), '26.02d')}}"
}
]
}
@@ -80,12 +80,12 @@
{
"system": "{{? iif(snomedct_122869004_ncit.empty().not(), 'http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl')}}",
"code": "{{? snomedct_122869004_ncit}}",
- "version": "{{? iif(snomedct_122869004_ncit.empty().not(), '24.01e')}}"
+ "version": "{{? iif(snomedct_122869004_ncit.empty().not(), '26.02d')}}"
},
{
"system": "{{? iif(snomedct_122869004_snomed.empty().not(), 'http://snomed.info/sct')}}",
"code": "{{? snomedct_122869004_snomed}}",
- "version": "{{? iif(snomedct_122869004_snomed.empty().not(), 'SNOMEDCT_US_2024_09_01')}}"
+ "version": "{{? iif(snomedct_122869004_snomed.empty().not(), '2025AB')}}"
}
],
"text": "{{? iif(snomedct_122869004_snomed.empty().not(), 'Measurement - Procedure')}}"
diff --git a/src/rarelink/tofhir/mappings/ips.measurement.radiology.json b/src/rarelink/tofhir/mappings/ips.measurement.radiology.json
index 98887e3b6..d93201e46 100644
--- a/src/rarelink/tofhir/mappings/ips.measurement.radiology.json
+++ b/src/rarelink/tofhir/mappings/ips.measurement.radiology.json
@@ -43,7 +43,7 @@
{
"system": "{{'https://loinc.org/'}}",
"code": "{{ncit_c60819}}",
- "version": "{{'LNC278'}}"
+ "version": "{{'v281'}}"
}
],
"text": "{{'Measurements - Assay'}}"
@@ -70,7 +70,7 @@
{
"system": "{{? iif(ncit_c41255.empty().not(), 'https://ncit.nci.nih.gov')}}",
"code": "{{? ncit_c41255.substring(10)}}",
- "version": "{{? iif(ncit_c41255.empty().not(), '24.01e')}}"
+ "version": "{{? iif(ncit_c41255.empty().not(), '26.02d')}}"
}
]
}
@@ -80,12 +80,12 @@
{
"system": "{{? iif(snomedct_122869004_ncit.empty().not(), 'https://ncit.nci.nih.gov')}}",
"code": "{{? snomedct_122869004_ncit}}",
- "version": "{{? iif(snomedct_122869004_ncit.empty().not(), '24.01e')}}"
+ "version": "{{? iif(snomedct_122869004_ncit.empty().not(), '26.02d')}}"
},
{
"system": "{{? iif(snomedct_122869004_snomed.empty().not(), 'http://snomed.info/sct')}}",
"code": "{{? snomedct_122869004_snomed}}",
- "version": "{{? iif(snomedct_122869004_snomed.empty().not(), 'SNOMEDCT_US_2024_09_01')}}"
+ "version": "{{? iif(snomedct_122869004_snomed.empty().not(), '2025AB')}}"
}
],
"text": "{{? iif(snomedct_122869004_snomed.empty().not(), 'Measurement - Procedure')}}"
diff --git a/src/rarelink/tofhir/mappings/ips.patient.json b/src/rarelink/tofhir/mappings/ips.patient.json
index d584aed3f..3a0c1944c 100755
--- a/src/rarelink/tofhir/mappings/ips.patient.json
+++ b/src/rarelink/tofhir/mappings/ips.patient.json
@@ -48,7 +48,7 @@
"coding": [
{
"system": "{{'http://snomed.info/sct'}}",
- "version": "{{'SNOMEDCT_US_2024_09_01'}}",
+ "version": "{{'2025AB'}}",
"code": "{{'422549004'}}",
"display": "{{'Patient-related Identification code (observable entity)'}}"
}
@@ -92,7 +92,7 @@
"coding": [
{
"system": "{{? iif(%rarelinkpersonalinformation.snomedct_370159000.empty().not(), 'http://snomed.info/sct')}}",
- "version": "{{? iif(%rarelinkpersonalinformation.snomedct_370159000.empty().not(), 'SNOMEDCT_US_2024_09_01')}}",
+ "version": "{{? iif(%rarelinkpersonalinformation.snomedct_370159000.empty().not(), '2025AB')}}",
"code": "{{? iif(%rarelinkpersonalinformation.snomedct_370159000.empty().not(), '370159000')}}",
"display": "{{? iif(%rarelinkpersonalinformation.snomedct_370159000.empty().not(), 'Country of Birth')}}"
}
@@ -110,7 +110,7 @@
"coding": [
{
"system": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"code": "399423000",
"display": "Date of Admission"
}
@@ -132,7 +132,7 @@
"coding": [
{
"system": "{{? iif(%rarelinkpersonalinformation.loinc_76689_9.empty().not(), 'http://snomed.info/sct')}}",
- "version": "{{? iif(%rarelinkpersonalinformation.loinc_76689_9.empty().not(), 'SNOMEDCT_US_2024_09_01')}}",
+ "version": "{{? iif(%rarelinkpersonalinformation.loinc_76689_9.empty().not(), '281')}}",
"code": "{{? %rarelinkpersonalinformation.mpp:getConcept(%sexatbirth, loinc_76689_9, 'target_code')}}",
"display": "{{? %rarelinkpersonalinformation.mpp:getConcept(%sexatbirth, loinc_76689_9, 'target_display')}}"
}
@@ -145,7 +145,7 @@
"coding": [
{
"system": "{{? iif(%rarelinkpersonalinformation.loinc_76689_9.empty().not(), 'http://snomed.info/sct')}}",
- "version": "{{? iif(%rarelinkpersonalinformation.loinc_76689_9.empty().not(), 'SNOMEDCT_US_2024_09_01')}}",
+ "version": "{{? iif(%rarelinkpersonalinformation.loinc_76689_9.empty().not(), '281')}}",
"code": "{{? iif(%rarelinkpersonalinformation.loinc_76689_9.empty().not(), '281053000')}}",
"display": "{{? iif(%rarelinkpersonalinformation.loinc_76689_9.empty().not(), 'Sex at Birth')}}"
}
@@ -163,7 +163,7 @@
"coding": [
{
"system": "{{? iif(%RareLinkPatientStatus.snomedct_184305005.empty().not(), 'https://www.snomed.org/snomed-ct')}}",
- "version": "{{? iif(%RareLinkPatientStatus.snomedct_184305005.empty().not(), 'SNOMEDCT_US_2024_09_01')}}",
+ "version": "{{? iif(%RareLinkPatientStatus.snomedct_184305005.empty().not(), '2025AB')}}",
"code": "{{? iif(%RareLinkPatientStatus.snomedct_184305005.empty().not(), '184305005')}}",
"display": "{{? iif(%RareLinkPatientStatus.snomedct_184305005.empty().not(), 'Cause Of Death')}}"
}
diff --git a/src/rarelink/tofhir/mappings/ips.procedure.json b/src/rarelink/tofhir/mappings/ips.procedure.json
index bd8a0776c..8b93605e4 100644
--- a/src/rarelink/tofhir/mappings/ips.procedure.json
+++ b/src/rarelink/tofhir/mappings/ips.procedure.json
@@ -30,7 +30,7 @@
{
"code": "{{snomedct_122869004}}",
"system": "{{iif(snomedct_122869004.empty().not(), 'http://hl7.org/fhir/uv/ips/ValueSet/procedures-uv-ips')}}",
- "version": "{{iif(snomedct_122869004.empty().not(), 'SNOMEDCT_US_2024_09_01')}}"
+ "version": "{{iif(snomedct_122869004.empty().not(), '2025AB')}}"
}
]
},
@@ -42,7 +42,7 @@
{
"code": "{{snomedct_122869004_bdsite}}",
"system": "{{iif(snomedct_122869004_bdsite.empty().not(), 'http://snomed.info/sct')}}",
- "version": "{{iif(snomedct_122869004_bdsite.empty().not(), 'SNOMEDCT_US_2024_09_01')}}"
+ "version": "{{iif(snomedct_122869004_bdsite.empty().not(), '2025AB')}}"
}
]
}
diff --git a/src/rarelink/tofhir/mappings/observation.age_category.json b/src/rarelink/tofhir/mappings/observation.age_category.json
index 6fb1d2b37..f338399cb 100644
--- a/src/rarelink/tofhir/mappings/observation.age_category.json
+++ b/src/rarelink/tofhir/mappings/observation.age_category.json
@@ -31,7 +31,7 @@
{
"code": "{{'105727008'}}",
"system": "{{'http://snomed.info/sct'}}",
- "version": "{{'SNOMEDCT_US_2024_09_01'}}",
+ "version": "{{'2025AB'}}",
"display": "{{'Age Category'}}"
}
]
@@ -43,7 +43,7 @@
{
"code": "{{? mpp:getConcept(%ageCategory, snomedct_105727008, 'target_code')}}",
"system": "{{'http://snomed.info/sct'}}",
- "version": "{{'SNOMEDCT_US_2024_09_01'}}",
+ "version": "{{'2025AB'}}",
"display": "{{? mpp:getConcept(%ageCategory, snomedct_105727008, 'target_display')}}"
}
]
diff --git a/src/rarelink/tofhir/mappings/observation.karyotypic_sex.json b/src/rarelink/tofhir/mappings/observation.karyotypic_sex.json
index 9174af569..e849ebdd8 100644
--- a/src/rarelink/tofhir/mappings/observation.karyotypic_sex.json
+++ b/src/rarelink/tofhir/mappings/observation.karyotypic_sex.json
@@ -31,7 +31,7 @@
{
"code": "{{'1296886006'}}",
"system": "{{'http://snomed.info/sct'}}",
- "version": "{{'SNOMEDCT_US_2024_09_01'}}",
+ "version": "{{'2025AB'}}",
"display": "{{'Karyotypic Sex'}}"
}
]
@@ -42,7 +42,7 @@
{
"code": "{{? mpp:getConcept(%karyotypicSexConceptMap, snomedct_1296886006, 'target_code')}}",
"system": "{{'http://snomed.info/sct'}}",
- "version": "{{'SNOMEDCT_US_2024_09_01'}}",
+ "version": "{{'2025AB'}}",
"display": "{{? mpp:getConcept(%karyotypicSexConceptMap, snomedct_1296886006, 'target_display')}}"
}
]
diff --git a/src/rarelink/tofhir/mappings/observation.length_of_gestation_at_birth.json b/src/rarelink/tofhir/mappings/observation.length_of_gestation_at_birth.json
index d35ab311e..2d61d0cb7 100644
--- a/src/rarelink/tofhir/mappings/observation.length_of_gestation_at_birth.json
+++ b/src/rarelink/tofhir/mappings/observation.length_of_gestation_at_birth.json
@@ -31,7 +31,7 @@
{
"code": "{{'412726003'}}",
"system": "{{'http://snomed.info/sct'}}",
- "version": "{{'SNOMEDCT_US_2024_09_01'}}",
+ "version": "{{'2025AB'}}",
"display": "{{'Length of Gestation at Birth - weeks+days'}}"
}
]
@@ -45,7 +45,7 @@
{
"code": "{{'412726003'}}",
"system": "{{'http://snomed.info/sct'}}",
- "version": "{{'SNOMEDCT_US_2024_09_01'}}",
+ "version": "{{'2025AB'}}",
"display": "{{'Length of Gestation at Birth - weeks'}}"
}
]
@@ -63,7 +63,7 @@
{
"code": "{{'412726003'}}",
"system": "{{'http://snomed.info/sct'}}",
- "version": "{{'SNOMEDCT_US_2024_09_01'}}",
+ "version": "{{'2025AB'}}",
"display": "{{'Length of Gestation at Birth - days'}}"
}
]
diff --git a/src/rarelink/tofhir/mappings/observation.measurements.other.json b/src/rarelink/tofhir/mappings/observation.measurements.other.json
index 0217dc27f..ef50bbb49 100644
--- a/src/rarelink/tofhir/mappings/observation.measurements.other.json
+++ b/src/rarelink/tofhir/mappings/observation.measurements.other.json
@@ -41,7 +41,7 @@
"coding": [
{
"system": "{{'http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl'}}",
- "version": "{{'24.01e'}}",
+ "version": "{{'26.02d'}}",
"code": "{{'ncit_c60819'}}"
}
]
@@ -58,7 +58,7 @@
"coding": [
{
"system": "{{? iif(ncit_c41255.empty().not(), 'http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl')}}",
- "version": "{{? iif(ncit_c41255.empty().not(), '24.01e')}}",
+ "version": "{{? iif(ncit_c41255.empty().not(), '26.02d')}}",
"code": "{{? ncit_c41255.substring(10)}}"
}
]
@@ -68,12 +68,12 @@
"coding": [
{
"system": "{{? iif(snomedct_122869004_ncit.empty().not(), 'http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl')}}",
- "version": "{{? iif(snomedct_122869004_ncit.empty().not(), '24.01e')}}",
+ "version": "{{? iif(snomedct_122869004_ncit.empty().not(), '26.02d')}}",
"code": "{{? snomedct_122869004_ncit}}"
},
{
"system": "{{? iif(snomedct_122869004_snomed.empty().not(), 'http://snomed.info/sct')}}",
- "version": "{{? iif(snomedct_122869004_snomed.empty().not(), 'SNOMEDCT_US_2024_09_01')}}",
+ "version": "{{? iif(snomedct_122869004_snomed.empty().not(), '2025AB')}}",
"code": "{{? snomedct_122869004_snomed}}"
}
]
diff --git a/src/rarelink/tofhir/mappings/observation.phenotypic_feature.json b/src/rarelink/tofhir/mappings/observation.phenotypic_feature.json
index d86967e31..c0ff72754 100644
--- a/src/rarelink/tofhir/mappings/observation.phenotypic_feature.json
+++ b/src/rarelink/tofhir/mappings/observation.phenotypic_feature.json
@@ -30,7 +30,7 @@
"coding": [
{
"system": "{{'http://purl.obolibrary.org/obo/hp.owl'}}",
- "version": "{{'2025-05-06'}}",
+ "version": "{{'2026-02-16'}}",
"code": "{{? snomedct_8116006.substring(3)}}"
}
]
@@ -40,7 +40,7 @@
"coding": [
{
"system": "{{? iif(hp_0003674.empty().not(), 'http://purl.obolibrary.org/obo/hp.owl')}}",
- "version": "{{? iif(hp_0003674.empty().not(), '2025-05-06')}}",
+ "version": "{{? iif(hp_0003674.empty().not(), '2026-02-16')}}",
"code": "{{? mpp:getConcept(%phenotypeAgeOfOnset, hp_0003674, 'target_code')}}",
"display": "{{? mpp:getConcept(%phenotypeAgeOfOnset, hp_0003674, 'target_display')}}"
}
@@ -57,7 +57,7 @@
"coding": [
{
"system": "{{? iif(hp_0012823_snomed.empty().not(), 'http://snomed.info/sct')}}",
- "version": "{{? iif(hp_0012823_snomed.empty().not(), 'SNOMEDCT_US_2024_09_01')}}",
+ "version": "{{? iif(hp_0012823_snomed.empty().not(), '2025AB')}}",
"code": "{{? hp_0012823_snomed}}"
}
],
@@ -80,7 +80,7 @@
"coding": [
{
"system": "{{? iif(snomedct_363778006.empty().not(), 'http://snomed.info/sct')}}",
- "version": "{{? iif(snomedct_363778006.empty().not(), 'SNOMEDCT_US_2024_09_01')}}",
+ "version": "{{? iif(snomedct_363778006.empty().not(), '2025AB')}}",
"code": "{{? mpp:getConcept(%phenotypeStatus, snomedct_363778006, 'target_code')}}",
"display": "{{? mpp:getConcept(%phenotypeStatus, snomedct_363778006 , 'target_display')}}"
}
@@ -99,7 +99,7 @@
"coding": [
{
"system": "{{? iif(hp_0011008.empty().not(), 'http://purl.obolibrary.org/obo/hp.owl')}}",
- "version": "{{? iif(hp_0011008.empty().not(), '2025-05-06')}}",
+ "version": "{{? iif(hp_0011008.empty().not(), '2026-02-16')}}",
"code": "{{? mpp:getConcept(%phenotypeTemporalPattern, hp_0011008, 'target_code')}}",
"display": "{{? mpp:getConcept(%phenotypeTemporalPattern, hp_0011008, 'target_display')}}"
}
@@ -112,7 +112,7 @@
"coding": [
{
"system": "{{? iif(hp_0012824.empty().not(), 'http://purl.obolibrary.org/obo/hp.owl')}}",
- "version": "{{? iif(hp_0012824.empty().not(), '2025-05-06')}}",
+ "version": "{{? iif(hp_0012824.empty().not(), '2026-02-16')}}",
"code": "{{? mpp:getConcept(%phenotypeSeverity, hp_0012824, 'target_code')}}",
"display": "{{? mpp:getConcept(%phenotypeSeverity, hp_0012824, 'target_display')}}"
}
@@ -125,7 +125,7 @@
"coding": [
{
"system": "{{? iif(hp_0012823_hp1.empty().not(), 'http://purl.obolibrary.org/obo/hp.owl')}}",
- "version": "{{? iif(hp_0012823_hp1.empty().not(), '2025-05-06')}}",
+ "version": "{{? iif(hp_0012823_hp1.empty().not(), '2026-02-16')}}",
"code": "{{? hp_0012823_hp1.substring(3))}}"
}
]
@@ -137,7 +137,7 @@
"coding": [
{
"system": "{{? iif(hp_0012823_hp2.empty().not(), 'http://purl.obolibrary.org/obo/hp.owl')}}",
- "version": "{{? iif(hp_0012823_hp2.empty().not(), '2025-05-06')}}",
+ "version": "{{? iif(hp_0012823_hp2.empty().not(), '2026-02-16')}}",
"code": "{{? hp_0012823_hp2.substring(3))}}"
}
]
@@ -149,7 +149,7 @@
"coding": [
{
"system": "{{? iif(hp_0012823_hp3.empty().not(), 'http://purl.obolibrary.org/obo/hp.owl')}}",
- "version": "{{? iif(hp_0012823_hp3.empty().not(), '2025-05-06')}}",
+ "version": "{{? iif(hp_0012823_hp3.empty().not(), '2026-02-16')}}",
"code": "{{? hp_0012823_hp3.substring(3))}}"
}
]
diff --git a/src/rarelink/tofhir/mappings/observation.vitalsigns.json b/src/rarelink/tofhir/mappings/observation.vitalsigns.json
index 1aa3d05a6..b5e3d6522 100644
--- a/src/rarelink/tofhir/mappings/observation.vitalsigns.json
+++ b/src/rarelink/tofhir/mappings/observation.vitalsigns.json
@@ -42,13 +42,13 @@
{
"system": "{{? iif(ln_85353_1.empty().not(), 'http ://loinc.org')}}",
"code": "{{? mpp:getConcept(%VitalSignPanel, ln_85353_1, 'target_code')}}",
- "version": "{{? iif(ln_85353_1.empty().not(), 'LNC278')}}",
+ "version": "{{? iif(ln_85353_1.empty().not(), 'v281')}}",
"display": "{{? mpp:getConcept(%VitalSignPanel, ln_85353_1, 'target_display')}}"
},
{
"system": "{{? iif(ln_85353_1_other.empty().not(), 'http ://loinc.org')}}",
"code": "{{? ln_85353_1_other}}",
- "version": "{{? iif(ln_85353_1_other.empty().not(), 'LNC278')}}"
+ "version": "{{? iif(ln_85353_1_other.empty().not(), 'v281')}}"
}
]
},
@@ -64,7 +64,7 @@
{
"system": "{{? iif(ncit_c41255.empty().not(), 'http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl')}}",
"code": "{{? ncit_c41255.substring(10)}}",
- "version": "{{? iif(ncit_c41255.empty().not(), '24.01e')}}"
+ "version": "{{? iif(ncit_c41255.empty().not(), '26.02d')}}"
}
]
}
@@ -74,12 +74,12 @@
{
"system": "{{? iif(snomedct_122869004_ncit.empty().not(), 'http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl')}}",
"code": "{{? snomedct_122869004_ncit.substring(10)}}",
- "version": "{{? iif(snomedct_122869004_ncit.empty().not(), '24.01e')}}"
+ "version": "{{? iif(snomedct_122869004_ncit.empty().not(), '26.02d')}}"
},
{
"system": "{{? iif(snomedct_122869004_snomed.empty().not(), 'http://snomed.info/sct')}}",
"code": "{{? snomedct_122869004_snomed.substring(7)}}",
- "version": "{{? iif(snomedct_122869004_snomed.empty().not(), 'SNOMEDCT_US_2024_09_01')}}"
+ "version": "{{? iif(snomedct_122869004_snomed.empty().not(), '2025AB')}}"
}
]
},
diff --git a/tests/phenopackets/test_data/101.json b/tests/phenopackets/test_data/101.json
index 4be0fd66d..e3e2a88d4 100644
--- a/tests/phenopackets/test_data/101.json
+++ b/tests/phenopackets/test_data/101.json
@@ -453,7 +453,7 @@
"id": "mondo",
"name": "Monarch Disease Ontology",
"url": "https://purl.obolibrary.org/obo/MONDO/",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"namespace_prefix": "MONDO",
"iri_prefix": "http://purl.obolibrary.org/obo/MONDO_"
},
@@ -461,7 +461,7 @@
"id": "hpo",
"name": "Human Phenotype Ontology",
"url": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"namespace_prefix": "HPO",
"iri_prefix": "http://purl.obolibrary.org/obo/HP_"
},
@@ -469,7 +469,7 @@
"id": "loinc",
"name": "Logical Observation Identifiers Names and Codes",
"url": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"namespace_prefix": "LOINC",
"iri_prefix": "http://loinc.org"
},
@@ -477,7 +477,7 @@
"id": "uo",
"name": "Units of Measurement Ontology",
"url": "https://www.ontobee.org/ontology/UO",
- "version": "2023-05-25",
+ "version": "2026-01-16",
"namespace_prefix": "UO",
"iri_prefix": "http://purl.obolibrary.org/obo/UO_"
},
@@ -509,7 +509,7 @@
"id": "geno",
"name": "GENO - The Genotype Ontology",
"url": "https://www.genoontology.org/",
- "version": "2023-10-08",
+ "version": "2026-02-02",
"namespace_prefix": "GENO",
"iri_prefix": "http://purl.obolibrary.org/obo/GENO_"
}
diff --git a/tests/phenopackets/test_data/102.json b/tests/phenopackets/test_data/102.json
index 85cb1edb8..73d98fcb2 100644
--- a/tests/phenopackets/test_data/102.json
+++ b/tests/phenopackets/test_data/102.json
@@ -238,7 +238,7 @@
"id": "snomedct",
"name": "Systematized Medical Nomenclature for Medicine\u2013Clinical Terminology",
"url": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"namespacePrefix": "SNOMEDCT",
"iriPrefix": "http://snomed.info/sct"
},
@@ -246,7 +246,7 @@
"id": "mondo",
"name": "Monarch Disease Ontology",
"url": "https://purl.obolibrary.org/obo/MONDO/",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"namespacePrefix": "MONDO",
"iriPrefix": "http://purl.obolibrary.org/obo/MONDO_"
},
@@ -254,7 +254,7 @@
"id": "hpo",
"name": "Human Phenotype Ontology",
"url": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"namespacePrefix": "HPO",
"iriPrefix": "http://purl.obolibrary.org/obo/HP_"
},
@@ -262,7 +262,7 @@
"id": "loinc",
"name": "Logical Observation Identifiers Names and Codes",
"url": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"namespacePrefix": "LOINC",
"iriPrefix": "http://loinc.org"
},
@@ -286,7 +286,7 @@
"id": "ncit",
"name": "NCI Thesaurus OBO Edition",
"url": "https://ncit.nci.nih.gov/",
- "version": "24.01e",
+ "version": "26.02d",
"namespacePrefix": "NCIT",
"iriPrefix": "http://purl.obolibrary.org/obo/NCIT_"
},
@@ -326,7 +326,7 @@
"id": "icd11",
"name": "International Classification of Diseases, Eleventh Revision",
"url": "https://icd.who.int/en",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"namespacePrefix": "ICD11",
"iriPrefix": "http://hl7.org/fhir/sid/icd-11"
},
@@ -350,7 +350,7 @@
"id": "geno",
"name": "GENO - The Genotype Ontology",
"url": "https://www.genoontology.org/",
- "version": "2023-10-08",
+ "version": "2026-02-02",
"namespacePrefix": "GENO",
"iriPrefix": "http://purl.obolibrary.org/obo/GENO_"
},
diff --git a/tests/phenopackets/test_data/103.json b/tests/phenopackets/test_data/103.json
index 6c3c54d96..48d314f6b 100644
--- a/tests/phenopackets/test_data/103.json
+++ b/tests/phenopackets/test_data/103.json
@@ -375,7 +375,7 @@
"id": "snomedct",
"name": "Systematized Medical Nomenclature for Medicine\u2013Clinical Terminology",
"url": "http://snomed.info/sct",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"namespacePrefix": "SNOMEDCT",
"iriPrefix": "http://snomed.info/sct"
},
@@ -383,7 +383,7 @@
"id": "mondo",
"name": "Monarch Disease Ontology",
"url": "https://purl.obolibrary.org/obo/MONDO/",
- "version": "2025-06-03",
+ "version": "2026-03-03",
"namespacePrefix": "MONDO",
"iriPrefix": "http://purl.obolibrary.org/obo/MONDO_"
},
@@ -391,7 +391,7 @@
"id": "hpo",
"name": "Human Phenotype Ontology",
"url": "http://purl.obolibrary.org/obo/hp.owl",
- "version": "2025-05-06",
+ "version": "2026-02-16",
"namespacePrefix": "HPO",
"iriPrefix": "http://purl.obolibrary.org/obo/HP_"
},
@@ -399,7 +399,7 @@
"id": "loinc",
"name": "Logical Observation Identifiers Names and Codes",
"url": "https://loinc.org",
- "version": "LNC278",
+ "version": "v281",
"namespacePrefix": "LOINC",
"iriPrefix": "http://loinc.org"
},
@@ -423,7 +423,7 @@
"id": "ncit",
"name": "NCI Thesaurus OBO Edition",
"url": "https://ncit.nci.nih.gov/",
- "version": "24.01e",
+ "version": "26.02d",
"namespacePrefix": "NCIT",
"iriPrefix": "http://purl.obolibrary.org/obo/NCIT_"
},
@@ -463,7 +463,7 @@
"id": "icd11",
"name": "International Classification of Diseases, Eleventh Revision",
"url": "https://icd.who.int/en",
- "version": "SNOMEDCT_US_2024_09_01",
+ "version": "2025AB",
"namespacePrefix": "ICD11",
"iriPrefix": "http://hl7.org/fhir/sid/icd-11"
},
@@ -487,7 +487,7 @@
"id": "geno",
"name": "GENO - The Genotype Ontology",
"url": "https://www.genoontology.org/",
- "version": "2023-10-08",
+ "version": "2026-02-02",
"namespacePrefix": "GENO",
"iriPrefix": "http://purl.obolibrary.org/obo/GENO_"
},
diff --git a/tests/phenopackets/test_data/sample_records_rarelink_cdm.json b/tests/phenopackets/test_data/sample_records_rarelink_cdm.json
index 23f2067e0..6484c982b 100644
--- a/tests/phenopackets/test_data/sample_records_rarelink_cdm.json
+++ b/tests/phenopackets/test_data/sample_records_rarelink_cdm.json
@@ -146,7 +146,7 @@
"snomedct_424850005": "",
"snomedct_298059007": "",
"snomedct_423493009": "snomedct_410672004",
- "snomedct_432213005": "SNOMEDCT_US_2024_09_01",
+ "snomedct_432213005": "2025AB",
"snomedct_363698007": "",
"snomedct_263493007": "hl7fhir_active",
"snomedct_246112005": "snomedct_24484000",