Term information
- Orphanet:309279 (MONDO:equivalentTo)
- UMLS:C5681075 (MONDO:equivalentTo)
- GARD:10670 (MONDO:GARD)
- icd11.foundation:979972142 (Orphanet:309279)
- MEDGEN:1842769 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, disease_grouping, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, mondo_top_grouping_hereditary_disease, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, mondo_top_grouping_metabolic_disease, matrix_txgnn_grouping_metabolic_disease, matrix_txgnn_grouping_member, rare, harrisons_view_member, harrisons_view_hereditary_disease, ordo_group_of_disorders, harrisons_view_metabolic_disease
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/979972142
http://www.orpha.net/ORDO/Orphanet_309279
http://linkedlifedata.com/resource/umls/id/C5681075
http://identifiers.org/medgen/1842769