Disease #06195 (CMS25 (Myasthenic syndrome, congenital, 25), OMIM:618323)
| Official abbreviation |
CMS25 |
| Name |
Myasthenic syndrome, congenital, 25 |
| OMIM ID |
618323 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
VAMP1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|