Charcot-Marie-Tooth disease, type 4H Gene Set

Dataset ClinVar Gene-Phenotype 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
Similar Terms
Downloads & Tools

Genes

1 genes associated with the Charcot-Marie-Tooth disease, type 4H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
FGD4 FYVE, RhoGEF and PH domain containing 4