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Search diseases:
OMIM ID
144010
OMIM term:
HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B
Alternative terms:
APOLIPOPROTEIN B-100, FAMILIAL LIGAND-DEFECTIVE
HYPERCHOLESTEROLEMIA, FAMILIAL, DUE TO LIGAND-DEFECTIVE APOLIPOPROTEIN B
APOLIPOPROTEIN B-100, FAMILIAL DEFECTIVE
(∗) Location:
2p24.1
(†) Associated OMIM genes:
APOB LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 4, INCLUDED; LDLCQ4, INCLUDED
(‡) Associated MGI genes:
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