Term information
- MEDGEN:1826137 (MONDO:equivalentTo)
- UMLS:C5781874 (MONDO:equivalentTo)
- DOID:0081358 (MONDO:equivalentTo)
- OMIM:113800 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, mondo_top_grouping_integumentary_system_disorder, matrix_llm__tag_qualy_lost_other, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_included, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, harrisons_view_hereditary_disease, mondo_top_grouping_disorder_of_development_or_morphogenesis, harrisons_view_integumentary_system_disorder
http://purl.obolibrary.org/obo/DOID_0081358
http://identifiers.org/medgen/1826137
http://linkedlifedata.com/resource/umls/id/C5781874
https://omim.org/entry/113800