Disease #03846 (MDDGA11 (dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A11 (MDDGA-11)), OMIM:615181)

Official abbreviation MDDGA11
Name dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A11 (MDDGA-11)
OMIM ID 615181
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene B3GALNT2
Associated tissues -
Disease features -
Remarks -