An inherited metabolic disorder caused by an enzyme deficiency, resulting in an inability to oxidize fatty acids for energy production. [ NCIT:C97092 ]

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:272.8 (i2s)
  • Orphanet:309005 (MONDO:equivalentTo)
  • UMLS:C0154251 (Orphanet:309005)
  • DOID:3146 (MONDO:equivalentTo)
  • NCIT:C97092 (MONDO:equivalentTo)
  • MedDRA:10061227 (Orphanet:309005)
  • ICD9:272.9 (i2s)
  • SCTID:267431006 (MONDO:equivalentTo)
Subsets

ordo_group_of_disorders

closeMatch

http://identifiers.org/mesh/D008052

http://linkedlifedata.com/resource/umls/id/C0023772

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/specific_disease_by_disrupted_process.yaml

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://www.orpha.net/ORDO/Orphanet_309005

http://purl.obolibrary.org/obo/NCIT_C97092

http://identifiers.org/meddra/10061227

http://identifiers.org/snomedct/267431006

has broad synonym

lipid metabolism disorder

disorder of lipid metabolism

dyslipidemia

has related synonym

fatty acid metabolism disorder

id

MONDO:0002525