RS201689565 SPG11
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What This Variant Does
"CLNSIG=4
Associated Conditions
Difficulty walking
Spastic paraparesis
Generalized hyperreflexia
Gait disturbance
Hereditary spastic paraplegia 11
Hereditary spastic paraplegia
Amyotrophic lateral sclerosis
Inborn genetic diseases
Juvenile amyotrophic lateral sclerosis
Charcot-Marie-Tooth disease axonal type 2X
Amyotrophic lateral sclerosis type 5
Difficulty walking
Spastic paraparesis
Generalized hyperreflexia
Gait disturbance
Other Variants in SPG11