RS780898043 SETX
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Associated Conditions
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Amyotrophic lateral sclerosis type 4
Inborn genetic diseases
Cone-rod dystrophy
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Amyotrophic lateral sclerosis type 4
Inborn genetic diseases
Cone-rod dystrophy
Other Variants in SETX