RS145734191 SCN11A
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Associated Conditions
Hereditary sensory and autonomic neuropathy type 7
Familial episodic pain syndrome with predominantly lower limb involvement
Charcot-Marie-Tooth disease
Inborn genetic diseases
Hereditary sensory and autonomic neuropathy type 7
Familial episodic pain syndrome with predominantly lower limb involvement
Charcot-Marie-Tooth disease
Inborn genetic diseases
Other Variants in SCN11A