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inherited lipid metabolism disorder

^ http://purl.obolibrary.org/obo/MONDO_0002525

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

Term info

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

Term relations