Phenotype #0000154481

Global Variome shared LOVD

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

Individual ID	00206610
Associated disease	-
Phenotype details	small chin, prominent U waves and bigeminy, hypokalemia, symptoms disappeared 24h later. Decreasement of the amplitude of th CMAP following long execise test.
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	19y
Age/Onset	15y
Phenotype/Onset	steroid induced hypokalemic paralysis
Protein	-
Owner name	Ikuko Takeda
Database submission license	No license selected
Created by	Ikuko Takeda
Date created	2013-05-22 12:31:07 +02:00 (CEST)
Date last edited	N/A

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