Disease #00738 (HOKPP2 (paralysis, hypokalemic, periodic, type 2 (HOKPP-2)), OMIM:613345)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	HOKPP2
Name	paralysis, hypokalemic, periodic, type 2 (HOKPP-2)
OMIM ID	613345
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
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)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.