Disease #02454 (LGMDD1;LGMD1E (dystrophy, muscular, limb-girdle, autosomal dominant, type 1 (LGMD1E)), OMIM:603511)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	LGMDD1;LGMD1E
Name	dystrophy, muscular, limb-girdle, autosomal dominant, type 1 (LGMD1E)
OMIM ID	603511
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DNAJB6
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2024-01-12 20:45:48 +01:00 (CET)

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