Phenotype #0000119569

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00147010
Associated disease	LGMD2
Phenotype details	-
Diagnosis/Initial	dystrophy, muscular, limb-girdle, autosomal recessive
Diagnosis/Definite	LGMD-2I
Inheritance	Familial, autosomal recessive
Age/Examination	-
Age/Onset	-
Phenotype/Onset	-
Age/Diagnosis	-
Protein	-
Owner name	Tom Winder
Database submission license	No license selected
Created by	Tom Winder
Date created	2012-11-20 17:01:38 +01:00 (CET)
Date last edited	2012-11-20 20:17:24 +01:00 (CET)

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