Disease #05223 (CMS20 (myasthenic syndrome, congenital, type 20, presynaptic (CMS-20)), OMIM:617143)
| Official abbreviation |
CMS20 |
| Name |
myasthenic syndrome, congenital, type 20, presynaptic (CMS-20) |
| OMIM ID |
617143 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
6 |
| Phenotype entries for this disease |
6 |
| Associated with 1 gene |
SLC5A7 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2017-02-10 16:34:12 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|