Disease #01500 (HOKPP-1 (paralysis, hypokalemic, periodic, type 1 (HOKPP-1)), OMIM:170400)

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Official abbreviation	HOKPP-1
Name	paralysis, hypokalemic, periodic, type 1 (HOKPP-1)
OMIM ID	170400
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	CACNA1S, SCN4A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A