Disease #00738 (HOKPP2 (paralysis, hypokalemic, periodic, type 2 (HOKPP-2)), OMIM:613345)
Official abbreviation |
HOKPP2 |
Name |
paralysis, hypokalemic, periodic, type 2 (HOKPP-2) |
OMIM ID |
613345 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
SCN4A |
Associated tissues |
- |
Disease features |
autosomal dominant |
Remarks |
- |
|
|