Phenotype #0000087198

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00110723
Associated disease	HOKPP
Phenotype details	Hypokalemic Periodic Paralysis (familial)
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	D Qiang
Database submission license	No license selected
Created by	D Qiang
Date created	2014-02-14 05:54:58 +01:00 (CET)
Date last edited	2017-07-31 17:16:26 +02:00 (CEST)

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