Search Ontology:
Human Disease

hyperalphalipoproteinemia 1

Term ID
DOID:0111369
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
  • MESH:C564591
  • MIM:143470
  • NCI:C128806
  • SNOMEDCT_US_2023_03_01:238080004
  • UMLS_CUI:C0342883
Ontology
Human Disease   ( DOID:0111369 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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