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inherited lipid metabolism disorder

Go to external page 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 ]

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0154251 (MONDO:equivalentTo)
  • ICD9:272.9 (MONDO:i2s)
  • DOID:3146 (MONDO:equivalentTo)
  • NCIT:C97092 (MONDO:equivalentTo)
  • MedDRA:10061227 (Orphanet:309005/e)
  • MEDGEN:57587 (MONDO:equivalentTo)
  • GARD:21314 (MONDO:GARD)
  • Orphanet:309005 (MONDO:equivalentTo)
  • ICD9:272.8 (MONDO:relatedTo)
  • SCTID:267431006 (MONDO:equivalentTo)
Subsets

gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders

UK spelling synonym
dyslipidaemia

closeMatch

http://identifiers.org/meddra/10061227

conformsTo

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

exactMatch

http://linkedlifedata.com/resource/umls/id/C0154251

http://identifiers.org/medgen/57587

http://purl.obolibrary.org/obo/DOID_3146

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

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

http://identifiers.org/snomedct/267431006

has broad synonym

lipid metabolism disorder

disorder of lipid metabolism

dyslipidemia

dyslipidaemia

has related synonym

fatty acid metabolism disorder

id

MONDO:0002525