Disease #01111 (MDDGA5 (dystrophy-dystroglycanopathy, muscular, (congenital with brain and eye anomalies), type A5), OMIM:613153)

Global Variome shared LOVD

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Official abbreviation	MDDGA5
Name	dystrophy-dystroglycanopathy, muscular, (congenital with brain and eye anomalies), type A5
OMIM ID	613153
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FKRP
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2024-01-12 21:53:20 +01:00 (CET)

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