|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Charcot-Marie-Tooth disease, type 2B1 (CMT2B1, also referred to as CMT4C1) is an axonal CMT peripheral sensorimotor polyneuropathy. (Orphanet Rare Disease Ontology, Orphanet_98856)|
|Downloads & Tools|
1 genes associated with the charcot-marie-tooth disease, type 2b1 phenotype from the curated OMIM Gene-Disease Associations dataset.