Phenotype #0000153611

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00205430
Associated disease	LGMD
Phenotype details	elevated serum creatine phosphokinase (HP:0003236) 2,000
Diagnosis/Initial	limb-girdle muscular dystrophy
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	LGMD-1E
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Tom Winder
Database submission license
Created by	Johan den Dunnen
Date created	2013-07-01 17:54:49 +02:00 (CEST)
Date last edited	2013-07-05 14:30:33 +02:00 (CEST)

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