Term information
- GARD:19766 (MONDO:GARD)
- MEDGEN:1863613 (MONDO:equivalentTo)
- Orphanet:100094 (MONDO:equivalentTo)
- ICD10WHO:D44.8 (Orphanet:100094/specific)
- UMLS:C5848154 (MONDO:equivalentTo)
- icd11.foundation:1316827435 (https://orcid.org/0000-0002-3458-4839)
gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, disease_grouping, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, harrisons_view_endocrine_system_disorder, matrix_llm__txgnn_other, mondo_top_grouping_endocrine_system_disorder, matrix_included, matrix_llm__tag_existing_treatment_other, nord_rare, matrix_txgnn_grouping_endocrine_system_disorder, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, matrix_txgnn_grouping_member, rare, harrisons_view_member, ordo_group_of_disorders
Editor note: ORDO classifies as inherited but there are non-inherited forms such as Carney triad
https://icd.who.int/browse10/2019/en#/D44.8
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1316827435
http://www.orpha.net/ORDO/Orphanet_100094
http://identifiers.org/medgen/1863613
http://linkedlifedata.com/resource/umls/id/C5848154