Disease #04526 (MDDGC7;LGMD2U (dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C7 (LGMD-2U)), OMIM:616052)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MDDGC7;LGMD2U
Name	dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C7 (LGMD-2U)
OMIM ID	616052
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ISPD
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	2024-01-12 21:28:28 +01:00 (CET)

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