RS111033319 MT-TS1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial cytochrome c oxidase deficiency
Deafness
sensorineural
with neurologic features
Mitochondrial non-syndromic sensorineural hearing loss
MELAS syndrome
Rare genetic deafness
Mitochondrial complex IV deficiency
nuclear type 1
Mitochondrial disease
MERRF syndrome
Primary mitochondrial disorders
Mitochondrial cytochrome c oxidase deficiency
Deafness
sensorineural
Other Variants in MT-TS1