Disease #00141 (LGMD-2 (dystrophy, muscular, limb-girdle, autosomal recessive, type 2 (LGMD-2)))

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Official abbreviation	LGMD-2
Name	dystrophy, muscular, limb-girdle, autosomal recessive, type 2 (LGMD-2)
OMIM ID	-
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 8 genes	CAPN3, DYSF, FKRP, FKTN, SGCA, SGCB, SGCD, SGCG
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-06-10 21:06:19 +02:00 (CEST)
Date last edited	N/A