Disease #04639 (CMS11 (myasthenic syndrome, congenital, type 11, associated with acetylcholine receptor deficiency (CMS-11)), OMIM:616326)
Official abbreviation |
CMS11 |
Name |
myasthenic syndrome, congenital, type 11, associated with acetylcholine receptor deficiency (CMS-11) |
OMIM ID |
616326 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
5 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
RAPSN |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2015-09-23 10:25:23 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|