This is just here as a test because I lose it

Term information

database cross reference
  • icd11.foundation:292840069 (https://orcid.org/0000-0002-3458-4839)
  • ICD10CM:E23.0 (Orphanet:101957/specific)
  • Orphanet:101957 (MONDO:equivalentTo)
  • GARD:19801 (MONDO:GARD)
Subsets

matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, disease_grouping, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, harrisons_view_endocrine_system_disorder, mondo_top_grouping_member, mondo_top_grouping_endocrine_system_disorder, matrix_txgnn_grouping_endocrine_system_disorder, matrix_included, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, matrix_txgnn_grouping_member, rare, harrisons_view_member, ordo_group_of_disorders

comment

Editor note: in ORDO, Orphanet:101957 is classified as genetic, yet has acquired subtypes

exactMatch

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/292840069

http://www.orpha.net/ORDO/Orphanet_101957

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0015968

id

MONDO:0015127

Term relations