RS150571352 SPG11
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Associated Conditions
Hereditary spastic paraplegia 11
Intellectual disability
Amyotrophic lateral sclerosis type 5
Inborn genetic diseases
Hereditary spastic paraplegia
Charcot-Marie-Tooth disease axonal type 2X
Hereditary spastic paraplegia 11
Intellectual disability
Amyotrophic lateral sclerosis type 5
Inborn genetic diseases
Hereditary spastic paraplegia
Charcot-Marie-Tooth disease axonal type 2X
Other Variants in SPG11