|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Charcot-Marie-Tooth disease, type 4A (CMT4A) is a severe, early-onset form of demyelinating CMT peripheral sensorimotor polyneuropathy characterized by severe motor retardation and progressive scoliosis. (Orphanet Rare Disease Ontology, Orphanet_99948)|
|Downloads & Tools|
1 genes associated with the charcot-marie-tooth disease, type 4a phenotype from the curated OMIM Gene-Disease Associations dataset.
|GDAP1||ganglioside induced differentiation associated protein 1|