Disease #02734 (LGMD-2D (dystrophy, muscular, limb-girdle, type 2D (LGMD-2D)), OMIM:608099)

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	Curator: Johan T. den Dunnen

Official abbreviation	LGMD-2D
Name	dystrophy, muscular, limb-girdle, type 2D (LGMD-2D)
OMIM ID	608099
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SGCA
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A