RS104894621 PMP22
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What This Variant Does
"[OMIM:?]
Associated Conditions
DEJERINE-SOTTAS SYNDROME
AUTOSOMAL DOMINANT
Charcot-Marie-Tooth disease
type I
Inborn genetic diseases
type IA
PMP22-related disorder
Dejerine-Sottas disease
Charcot-Marie-Tooth disease
type I
Charcot-Marie-Tooth disease
type I
DEJERINE-SOTTAS SYNDROME
AUTOSOMAL DOMINANT
Charcot-Marie-Tooth disease
Other Variants in PMP22