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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00437023 - - - - - - - - - - - HOKPP1 - CACNA1S CACNA1S 1 1 Yunjian Zhang
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