Any nervous system disorder in which the cause of the disease is a variation in the KIF5A gene.
Comprehensive, easy-to-understand information about this condition
Checking for content...
No external resources available.
leukoencephalopathy, megalencephalic
MONDO:0000137
epilepsy, familial adult myoclonic
MONDO:0000160
encephalopathy, acute, infection-induced
MONDO:0000166
GLUT1 deficiency syndrome
MONDO:0000188
paraganglioma
MONDO:0000448
familial hemiplegic migraine
MONDO:0000700