Disease #04588 (CMT-2V (Charcot-Marie-Tooth disease?, axonal, type 2V (CMT-2V)), OMIM:616491)
| Official abbreviation |
CMT-2V |
| Name |
Charcot-Marie-Tooth disease?, axonal, type 2V (CMT-2V) |
| OMIM ID |
616491 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
NAGLU |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:23 +02:00 (CEST) |
| Date last edited |
N/A |
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