Charcot-Marie-Tooth Disease, Type 4H Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Charcot-Marie-Tooth disease, type 4H (CMT4H) is a demyelinating CMT peripheral sensorimotor polyneuropathy (Orphanet Rare Disease Ontology, Orphanet_99954)
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1 genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Type 4H from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
FGD4 FYVE, RhoGEF and PH domain containing 4 2.88009