Disease #03445 (MDDGC9;LGMDR16;LGMD2P (dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C9 (LGMDR16, LGMD2P)), OMIM:613818)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MDDGC9;LGMDR16;LGMD2P
Name	dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C9 (LGMDR16, LGMD2P)
OMIM ID	613818
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DAG1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2024-01-12 21:36:55 +01:00 (CET)

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