charcot-marie-tooth disease, type 4a Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
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1 genes associated with the charcot-marie-tooth disease, type 4a phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
GDAP1 ganglioside induced differentiation associated protein 1