[X] developmental anomaly of metabolic origin

Go to external page http://purl.obolibrary.org/obo/MONDO_0015327


This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C5680623 (MONDO:equivalentTo)
  • Orphanet:139009 (MONDO:equivalentTo)
  • MEDGEN:1826093 (MONDO:equivalentTo)
  • GARD:19900 (MONDO:GARD)
Subsets

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

exactMatch

http://linkedlifedata.com/resource/umls/id/C5680623

http://www.orpha.net/ORDO/Orphanet_139009

http://identifiers.org/medgen/1826093

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0015960

id

MONDO:0015327