All 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:

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/jiszrjnt