Disease #04313 (CMS2A (myasthenic syndrome, congenital, type 2A, slow-channel (CMS-2A)), OMIM:616313)
Official abbreviation |
CMS2A |
Name |
myasthenic syndrome, congenital, type 2A, slow-channel (CMS-2A) |
OMIM ID |
616313 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
CHRNB1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2015-08-28 20:26:29 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|