|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Charcot-Marie-Tooth disease, type 4H (CMT4H) is a demyelinating CMT peripheral sensorimotor polyneuropathy (Orphanet Rare Disease Ontology, Orphanet_99954)|
|Downloads & Tools|
1 genes/proteins associated with the disease Charcot-Marie-Tooth Disease, Type 4H from the curated CTD Gene-Disease Associations dataset.
|FGD4||FYVE, RhoGEF and PH domain containing 4||2.88009|