OBO ID: DOID:0111369
Term Name: hyperalphalipoproteinemia 1 Search Ontology:
Synonyms:
  • HALP1
Definition: A cholesterol-ester transfer protein deficiency characterized by elevated levels of alpha-lipoprotein in the blood that has_material_basis_in heterozygous mutation in the CETP gene on chromosome 16q13. (2)
References:
Ontology: Human Disease   ( DOID:0111369 )
Relationships
is a type of:
OTHER hyperalphalipoproteinemia 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CETP [High density lipoprotein cholesterol level QTL 10] 143470
Hyperalphalipoproteinemia 143470
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.