Disease #00734 (HYPP (paralysis, periodic, hyperkalemic (HYPP)), OMIM:170500)
Official abbreviation |
HYPP |
Name |
paralysis, periodic, hyperkalemic (HYPP) |
OMIM ID |
170500 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
8 |
Phenotype entries for this disease |
8 |
Associated with 1 gene |
SCN4A |
Associated tissues |
- |
Disease features |
autosomal dominant |
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
|