A congenital disorder (due to inherited enzyme abnormality) or acquired (due to failure of a metabolically important organ) disorder resulting from an abnormal metabolic process. [ NCIT:C3235 ]
Synonyms: metabolic disorder metabolic disease disorder of metabolic process metabolic process disease
Term information
- MESH:D008659 (MONDO:equivalentTo)
- ICD9:277.8 (MONDO:relatedTo)
- ICD9:277.9 (MONDO:i2s)
- EFO:0000589 (MONDO:equivalentTo)
- DOID:0014667 (MONDO:equivalentTo)
- SCTID:75934005 (MONDO:equivalentTo)
- UMLS:C0025517 (NCIT:C3235)
- ICD10CM:E70-E88 (https://orcid.org/0000-0002-4142-7153)
- NCIT:C3235 (MONDO:equivalentTo)
- ICD10WHO:E70-E90 (MONDO:equivalentTo)
harrisons_view, rare_grouping
https://icd.who.int/browse10/2019/en#/E70-E90
http://purl.obolibrary.org/obo/DOID_0014667
http://purl.bioontology.org/ontology/ICD10CM/E70-E88
http://purl.obolibrary.org/obo/NCIT_C3235
http://linkedlifedata.com/resource/umls/id/C0025517
http://identifiers.org/mesh/D008659
http://identifiers.org/snomedct/75934005