Term info
database cross reference
- MedDRA:10061227 (Orphanet:309005/e)
- ICD9:272.8 (MONDO:relatedTo)
- UMLS:C0154251 (Orphanet:309005/e)
- NCIT:C97092 (MONDO:equivalentTo)
- SCTID:267431006 (MONDO:equivalentTo)
- ICD9:272.9 (MONDO:i2s)
- Orphanet:309005 (MONDO:equivalentTo)
- DOID:3146 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
closeMatch
http://identifiers.org/meddra/10061227
definition
An inherited metabolic disorder caused by an enzyme deficiency, resulting in an inability to oxidize fatty acids for energy production.
exactMatch
http://linkedlifedata.com/resource/umls/id/C0154251, http://purl.obolibrary.org/obo/DOID_3146, http://purl.obolibrary.org/obo/NCIT_C97092, http://identifiers.org/snomedct/267431006, http://purl.obolibrary.org/obo/Orphanet_309005
has broad synonym
lipid metabolism disorder, disorder of lipid metabolism, dyslipidemia
has related synonym
fatty acid metabolism disorder
id
MONDO:0002525