Disease #02492 (LGMD-2E (dystrophy, muscular, limb-girdle, type 2E (LGMD-2E)), OMIM:604286)

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Official abbreviation	LGMD-2E
Name	dystrophy, muscular, limb-girdle, type 2E (LGMD-2E)
OMIM ID	604286
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SGCB
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A