This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0342745 (MONDO:equivalentTo)
  • GARD:21308 (MONDO:GARD)
  • SCTID:237963003 (MONDO:equivalentTo)
  • Orphanet:308467 (MONDO:equivalentTo)
  • MEDGEN:575203 (MONDO:equivalentTo)
  • icd11.foundation:1462194012 (https://orcid.org/0000-0002-4142-7153)
Subsets

gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, matrix_excluded, matrix_llm__tag_qualy_lost_other, disease_grouping, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, 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, harrisons_view_metabolic_disease, ordo_group_of_disorders

exactMatch

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1462194012

http://identifiers.org/snomedct/237963003

http://identifiers.org/medgen/575203

http://www.orpha.net/ORDO/Orphanet_308467

http://linkedlifedata.com/resource/umls/id/C0342745

id

MONDO:0017690