This is just here as a test because I lose it
Term information
database
cross reference
- OMIMPS:146590 (MONDO:equivalentTo)
- UMLS:C0263580 (MONDO:equivalentTo)
- MEDGEN:75527 (MONDO:equivalentTo)
Subsets
gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, matrix_excluded, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_integumentary_system_disorder, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_member, mondo_top_grouping_hereditary_disease, 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, harrisons_view_integumentary_system_disorder
exactMatch
https://omim.org/phenotypicSeries/PS146590
http://identifiers.org/medgen/75527
http://linkedlifedata.com/resource/umls/id/C0263580