Search Ontology:
Human Disease

cholesterol-ester transfer protein deficiency

Term ID
DOID:0111368
Synonyms
  • CEPT deficiency
  • familial hyperalphalipoproteinemia
Definition
A lipid metabolism disorder characterized by elevated levels of alpha-lipoprotein in the blood. https://www.ncbi.nlm.nih.gov/pubmed/168823
References
  • ORDO:79506
Ontology
Human Disease   ( DOID:0111368 )
Relationships
is a type of
has subtype
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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