RS119103267 MFN2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Charcot-Marie-Tooth disease
axonal
autosomal recessive
type 2a2b
Charcot-Marie-Tooth disease type 2A2
Charcot-Marie-Tooth disease type 2
Inborn genetic diseases
MFN2-related disorder
Peripheral axonal neuropathy
Neuropathy
hereditary motor and sensory
type 6A
Hereditary motor and sensory neuropathy with optic atrophy
type 2A
Multiple symmetric lipomatosis
Other Variants in MFN2