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

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Charcot-Marie-Tooth disease, type 4C (CMT4C) is a demyelinating CMT peripheral sensorimotor polyneuropathy with early-onset scoliosis or kyphoscoliosis. (Orphanet Rare Disease Ontology, Orphanet_99949)
External Link http://www.omim.org/entry/601596
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Genes

1 genes associated with the charcot-marie-tooth disease, type 4c phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SH3TC2 SH3 domain and tetratricopeptide repeats 2