| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Charcot-Marie-Tooth disease, type 4F (CMT4F) is a demyelinating CMT peripheral sensorimotor polyneuropathy. (Orphanet Rare Disease Ontology, Orphanet_99952) |
| External Link | http://www.omim.org/entry/614895 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the charcot-marie-tooth disease, type 4f phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| PRX | periaxin |
