Disease #05437 (HOKPP1 (paralysis, hypokalemic, periodic, type 1), OMIM:170400)
Official abbreviation |
HOKPP1 |
Name |
paralysis, hypokalemic, periodic, type 1 |
OMIM ID |
170400 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
CACNA1S |
Associated tissues |
- |
Disease features |
autosomal dominant |
Remarks |
- |
Date created |
2018-06-02 17:06:27 +02:00 (CEST) |
Date last edited |
2023-10-12 11:44:06 +02:00 (CEST) |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|