All diseases

OMIM ID
175780
OMIM term:
PORENCEPHALY 1; POREN1
Alternative terms:
HEMIPLEGIA, INFANTILE, WITH PORENCEPHALY PORENCEPHALY, TYPE 1; T1P
PORENCEPHALY, TYPE 1, AUTOSOMAL DOMINANT; ADT1P
(∗) Location:
13q34  
(†) Associated OMIM genes:
COL4A1  
(‡) Associated MGI genes:
Col4a1  

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* quick link - http://q.sanger.ac.uk/c3593jw8