OntologiesdoidclassesDOID:0111232   
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congenital muscular dystrophy-dystroglycanopathy type A9
http://purl.obolibrary.org/obo/DOID_0111232

A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in DAG1 on 3p21.31.

Exact Synonyms
congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A9
MDDGA9
Walker-Warburg syndrome or muscle-eye-brain disease DAG1-related
    class Information
    has_dbxref

    MIM:616538

    has_obo_namespace

    disease_ontology

    class Relations