Term information
- Orphanet:93436 (MONDO:equivalentTo)
- MEDGEN:1843369 (MONDO:equivalentTo)
- GARD:19194 (MONDO:GARD)
- UMLS:C4736195 (MONDO:equivalentTo)
- icd11.foundation:177141175 (https://orcid.org/0000-0001-5208-3432)
matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, disease_grouping, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, matrix_llm__txgnn_other, mondo_top_grouping_hereditary_disease, mondo_top_grouping_musculoskeletal_system_disorder, matrix_llm__tag_existing_treatment_other, 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, harrisons_view_hereditary_disease, ordo_group_of_disorders
http://www.orpha.net/ORDO/Orphanet_93436
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/177141175
http://identifiers.org/medgen/1843369
http://linkedlifedata.com/resource/umls/id/C4736195