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
|
|