Disease #02709 (CMT2K (Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2K), OMIM:607831)
| Official abbreviation |
CMT2K |
| Name |
Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2K |
| OMIM ID |
607831 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant, Autosomal recessive |
| Individuals reported having this disease |
7 |
| Phenotype entries for this disease |
5 |
| Associated with 2 genes |
GDAP1, JPH1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2024-09-26 08:42:49 +02:00 (CEST) |
Individuals
|