Disease #01002 (CMS4C (myasthenic syndrome, congenital, type 4C, associated with acetylcholine receptor deficiency (CMS-4C)), OMIM:608931)
Official abbreviation |
CMS4C |
Name |
myasthenic syndrome, congenital, type 4C, associated with acetylcholine receptor deficiency (CMS-4C) |
OMIM ID |
608931 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
11 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
CHRNE |
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
|