Term Name: hyperalphalipoproteinemia 1
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.
Ontology: Human Disease [DOID:0111369]   ( DOID:0111369 )

Relationships
is a type of: autosomal dominant disease cholesterol-ester transfer protein deficiency