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
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