charcot-marie-tooth disease, type 4b1 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Charcot-Marie-Tooth disease, type 4B1 (CMT4B1) is a severe early-onset demyelinating CMT peripheral sensorimotor polyneuropathy. (Orphanet Rare Disease Ontology, Orphanet_99955)
External Link http://www.omim.org/entry/601382
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Genes

1 genes associated with the charcot-marie-tooth disease, type 4b1 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
MTMR2 myotubularin related protein 2