RS374211312 CHCHD10
Upload your DNA to see your genotype for this variant.
Associated Conditions
Lower motor neuron syndrome with late-adult onset
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2
Autosomal dominant mitochondrial myopathy with exercise intolerance
Inborn genetic diseases
CHCHD10-related disorder
Lower motor neuron syndrome with late-adult onset
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2
Autosomal dominant mitochondrial myopathy with exercise intolerance
Inborn genetic diseases
CHCHD10-related disorder
Other Variants in CHCHD10