Phenotype #0000305994

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00414093
Associated disease	Healthy/Control
Phenotype details	developmental delay, muscle weakness limb-girdle pattern, muscle weakness distal, hyperCK emission
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Maartje Pennings
Database submission license
Created by	Johan den Dunnen
Date created	2022-07-27 10:49:59 +02:00 (CEST)
Date last edited	N/A

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