Disease #04569 (CMT2U (Charcot-Marie-Tooth disease, axonal, type 2U (CMT-2U)), OMIM:616280)
| Official abbreviation |
CMT2U |
| Name |
Charcot-Marie-Tooth disease, axonal, type 2U (CMT-2U) |
| OMIM ID |
616280 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
MARS |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:23 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|