[X] developmental anomaly of metabolic origin
Go to external page http://purl.obolibrary.org/obo/MONDO_0015327
Term information
- UMLS:C5680623 (MONDO:equivalentTo)
- Orphanet:139009 (MONDO:equivalentTo)
- MEDGEN:1826093 (MONDO:equivalentTo)
- GARD:19900 (MONDO:GARD)
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
http://linkedlifedata.com/resource/umls/id/C5680623
http://www.orpha.net/ORDO/Orphanet_139009
http://identifiers.org/medgen/1826093
Term relations
- [X] developmental defect during embryogenesis and disease caused by disruption of some metabolic process