Phenotype #0000079366

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00101145
Associated disease	GSD2
Phenotype details	mild, see paper ...; no neurological symptoms, progressive painless, mild leg weakness, difficulty rising from chair and from lying to sitting;
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	68y (68 years)
Age/Diagnosis	-
Age/Onset	65y
Phenotype/Onset	difficulty walking
Protein	-
Owner name	Arnold Reuser
Database submission license
Created by	Johan den Dunnen
Date created	2006-10-26 10:00:00 +02:00 (CEST)
Date last edited	2017-08-10 14:23:25 +02:00 (CEST)

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