Disease #01111

Official abbreviation MDDGA-5
Name dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A5 (MDDGA-5)
OMIM ID 613153
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene FKRP
Associated tissues -
Disease features -
Remarks -