Disease #00816 (MDDGA-6 (dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A6 (MDDGA-6)), OMIM:613154)

Official abbreviation MDDGA-6
Name dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A6 (MDDGA-6)
OMIM ID 613154
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene LARGE
Associated tissues -
Disease features -
Remarks -