Term information
- GARD:22138 (MONDO:GARD)
- icd11.foundation:677862301 (MONDO:equivalentTo)
- UMLS:C1290728 (MONDO:equivalentTo)
- Orphanet:521127 (MONDO:equivalentTo)
- MEDGEN:713081 (MONDO:equivalentTo)
ordo_disorder, gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, mondo_top_grouping_mouth_disorder, mondo_top_grouping_musculoskeletal_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_included, nord_rare, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, harrisons_view_musculoskeletal_system_disorder, mondo_top_grouping_radiation_induced_disorder, orphanet_rare
http://identifiers.org/medgen/713081
http://www.orpha.net/ORDO/Orphanet_521127
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/677862301
http://linkedlifedata.com/resource/umls/id/C1290728
http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql