Disease #01107 (MDDGA2;MEB;WWS (dystrophy-dystroglycanopathy, muscular, (congenital with brain and eye anomalies), type A2 (WWS, MEB)), OMIM:613150)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MDDGA2;MEB;WWS
Name	dystrophy-dystroglycanopathy, muscular, (congenital with brain and eye anomalies), type A2 (WWS, MEB)
OMIM ID	613150
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	POMT2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2024-01-12 21:42:03 +01:00 (CET)

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