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
|