Phenotype #0000257314

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	00361916
Associated disease	LGMDR2;LGMD2B
Phenotype details	Muscle weakness HP:0001324
Diagnosis/Initial	CMT1A
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	LGMD2B
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Ibrahim Sahin
Database submission license
Created by	Ibrahim Sahin
Date created	2021-04-12 11:57:34 +02:00 (CEST)
Date last edited	2021-04-12 13:39:30 +02:00 (CEST)

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