All diseases

OMIM ID
141500
OMIM term:
MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1
Alternative terms:
FHM
MHP1 MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA, INCLUDED
MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED
(∗) Location:
19p13.2  
(†) Associated OMIM genes:
CACNA1A  
(‡) Associated MGI genes:
Cacna1a  

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* quick link - http://q.sanger.ac.uk/00g0p313