Charcot-Marie-Tooth disease, Type 4A Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Charcot-Marie-Tooth disease, type 4A (CMT4A) is a severe, early-onset form of demyelinating CMT peripheral sensorimotor polyneuropathy characterized by severe motor retardation and progressive scoliosis. (Orphanet Rare Disease Ontology, Orphanet_99948)
External Link
Similar Terms
Downloads & Tools


1 genes/proteins associated with the disease Charcot-Marie-Tooth disease, Type 4A from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GDAP1 ganglioside induced differentiation associated protein 1 2.88009