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

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Charcot-Marie-Tooth disease, type 4H (CMT4H) is a demyelinating CMT peripheral sensorimotor polyneuropathy (Orphanet Rare Disease Ontology, Orphanet_99954)
External Link http://www.omim.org/entry/609311
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Genes

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

Symbol Name
FGD4 FYVE, RhoGEF and PH domain containing 4