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

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Charcot-Marie-Tooth disease, type 4F (CMT4F) is a demyelinating CMT peripheral sensorimotor polyneuropathy. (Orphanet Rare Disease Ontology, Orphanet_99952)
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1 genes associated with the charcot-marie-tooth disease, type 4f phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
PRX periaxin