MIGRAINE, FAMILIAL HEMIPLEGIC, 1 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=OMIM:141500
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Genes

1 genes/proteins associated with the disease MIGRAINE, FAMILIAL HEMIPLEGIC, 1 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit 2.88009