All diseases

OMIM ID
300125
OMIM term:
MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2
Alternative terms:
MGR2
MFTS
(∗) Location:
Xq  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/c2o4qh1w