Disease #03903 (MDDGA14 (dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A14 (MDDGA-14)), OMIM:615350)

Official abbreviation MDDGA14
Name dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A14 (MDDGA-14)
OMIM ID 615350
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 GMPPB
Associated tissues -
Disease features -
Remarks -