Disease #04318 (CMS4A (myasthenic syndrome, congenital, type 4A, slow-channel (CMS-4A)), OMIM:605809)
| Official abbreviation |
CMS4A |
| Name |
myasthenic syndrome, congenital, type 4A, slow-channel (CMS-4A) |
| OMIM ID |
605809 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant, Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
CHRNE |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-08-28 21:27:12 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|