charcot-marie-tooth disease, type 2b1 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/605588
Similar Terms
Downloads & Tools

Genes

1 genes associated with the charcot-marie-tooth disease, type 2b1 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
LMNA lamin A/C