Phenotype #0000321230

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00430433
Associated disease	NMD
Diagnosis/Initial	neuromuscular disorder
Diagnosis/Definite	-
Phenotype details	congenital myopathy, proximal muscle weakness
Inheritance	Familial, autosomal dominant
Age/Examination	58y (58 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2023-01-20 11:39:52 +01:00 (CET)
Date last edited	N/A

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