RS78644690 TBC1D24
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Associated Conditions
Familial infantile myoclonic epilepsy
Autosomal dominant nonsyndromic hearing loss 65
Inborn genetic diseases
Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
Developmental and epileptic encephalopathy
1
Familial infantile myoclonic epilepsy
Autosomal dominant nonsyndromic hearing loss 65
Inborn genetic diseases
Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
Developmental and epileptic encephalopathy
1
Other Variants in TBC1D24