Phenotype #0000326786

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00436663
Associated disease	LGMDR3;LGMD2D
Phenotype details	CK level 16,408U/L; proximal muscle atrophy, beginning in lower extremities, weakness muscles shoulder/arms
Diagnosis/Initial	limb-girdle muscular dystrophy
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	LGMDR3
Age/Examination	29y (29 years)
Age/Diagnosis	08y
Age/Onset	08y
Phenotype/Onset	-
Protein	-
Owner name	Nguyen Hoang
Database submission license	No license selected
Created by	Nguyen Hoang
Date created	2023-09-27 04:33:47 +02:00 (CEST)
Date last edited	2025-11-04 17:12:31 +01:00 (CET)

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