Phenotype #0000129665

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00164628
Associated disease	HOKPP
Phenotype details	-
Diagnosis/Initial	hypokalaemic periodic paralyses
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	hypokalaemic periodic paralyses
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Emil Gustavsson
Database submission license	No license selected
Created by	Emil Gustavsson
Date created	2018-06-02 01:55:50 +02:00 (CEST)
Date last edited	2018-06-02 17:08:34 +02:00 (CEST)

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