Search Ontology:

Human Disease

lipid metabolism disorder

Term ID

DOID:3146

Synonyms

dyslipidemia
fatty acid metabolism disorder

Definition

An inherited metabolic disorder that involves the creation and degradation of lipids. http://en.wikipedia.org/wiki/Lipid_metabolism

References

MESH:D008052
UMLS_CUI:C0023772

Ontology

Human Disease ( DOID:3146 )

Relationships

is a type of: inherited metabolic disorder

inherited metabolic disorder Show first 5 Terms
has subtype: carnitine palmitoyltransferase I deficiency carnitine palmitoyltransferase II deficiency carnitine-acylcarnitine translocase deficiency cholesterol-ester transfer protein deficiency chylomicron retention disease ... Show All 19 Terms

carnitine palmitoyltransferase I deficiency carnitine palmitoyltransferase II deficiency carnitine-acylcarnitine translocase deficiency cholesterol-ester transfer protein deficiency chylomicron retention disease CK syndrome familial hyperlipidemia hypolipoproteinemia lipoid proteinosis medium chain acyl-CoA dehydrogenase deficiency MEND syndrome mitochondrial short-chain enoyl-CoA hydratase 1 deficiency mitochondrial trifunctional protein deficiency multiple congenital anomalies-hypotonia-seizures syndrome Refsum disease short chain acyl-CoA dehydrogenase deficiency Smith-Lemli-Opitz syndrome steroid inherited metabolic disorder very long chain acyl-CoA dehydrogenase deficiency Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models