RS376712059 TBC1D24
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Associated Conditions
Rare genetic deafness
DOORS syndrome
Developmental and epileptic encephalopathy
16
Familial infantile myoclonic epilepsy
Autosomal recessive nonsyndromic hearing loss 86
Autosomal dominant nonsyndromic hearing loss 65
Inborn genetic diseases
1
Rare genetic deafness
DOORS syndrome
Developmental and epileptic encephalopathy
16
Familial infantile myoclonic epilepsy
Autosomal recessive nonsyndromic hearing loss 86
Other Variants in TBC1D24