Disease #00570 (CMS1A (myasthenic syndrome, congenital, type 1A, slow-channel (CMS-1A)), OMIM:601462)
| Official abbreviation |
CMS1A |
| Name |
myasthenic syndrome, congenital, type 1A, slow-channel (CMS-1A) |
| OMIM ID |
601462 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
CHRNA1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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