All diseases

OMIM ID
300049
OMIM term:
HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT
Alternative terms:
HETEROTOPIA, FAMILIAL NODULAR
PERIVENTRICULAR NODULAR HETEROTOPIA 1; PVNH1
NODULAR HETEROTOPIA, BILATERAL PERIVENTRICULAR; NHBP; BPNH HETEROTOPIA, PERIVENTRICULAR NODULAR, WITH FRONTOMETAPHYSEAL DYSPLASIA, INCLUDED
(∗) Location:
Xq28  
(†) Associated OMIM genes:
FLNA  
(‡) Associated MGI genes:
Flna  

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