RS145643238 SPG11
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Associated Conditions
Hereditary spastic paraplegia 11
Intellectual disability
Charcot-Marie-Tooth disease axonal type 2X
Inborn genetic diseases
Amyotrophic lateral sclerosis type 5
Thyroid cancer
nonmedullary
1
Malignant tumor of esophagus
SPG11-related disorder
Hereditary spastic paraplegia 11
Intellectual disability
Charcot-Marie-Tooth disease axonal type 2X
Inborn genetic diseases
Amyotrophic lateral sclerosis type 5
Other Variants in SPG11