All diseases

OMIM ID
607432
OMIM term:
LISSENCEPHALY 1; LIS1
Alternative terms:
LISSENCEPHALY SEQUENCE, ISOLATED; ILS
LISSENCEPHALY, CLASSIC SUBCORTICAL LAMINAR HETEROTOPIA, INCLUDED; SCLH, INCLUDED
SUBCORTICAL BAND HETEROTOPIA, INCLUDED; SBH, INCLUDED
(∗) Location:
17p13.3  
(†) Associated OMIM genes:
PAFAH1B1  
(‡) Associated MGI genes:
Dcx   Pafah1b1   Tuba1a  

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