Disease #00022 (MC (Myotonia Congenita), OMIM:160800)
| Official abbreviation |
MC |
| Name |
Myotonia Congenita |
| OMIM ID |
160800 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
114 |
| Phenotype entries for this disease |
- |
| Associated with 2 genes |
CLCN1, SCN4A |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
Individuals
|
|