Term information
- UMLS:C3266076 (MONDO:equivalentTo)
- MEDGEN:472000 (MONDO:equivalentTo)
- OMIMPS:119530 (https://orcid.org/0000-0002-6601-2165)
- SCTID:449790007 (MONDO:equivalentTo)
- DOID:0050567 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, mondo_top_grouping_musculoskeletal_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_member, harrisons_view_musculoskeletal_system_disorder, harrisons_view_hereditary_disease
https://omim.org/phenotypicSeries/PS119530
http://purl.obolibrary.org/obo/DOID_0050567
http://identifiers.org/medgen/472000
http://linkedlifedata.com/resource/umls/id/C3266076
http://identifiers.org/snomedct/449790007