{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014683", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014683", 
            "name": "Walker-Warburg syndrome or muscle-eye brain disease, Dag1-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014683", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014683", 
            "name": "MDDGA9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014683", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014683", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9; MDDGA9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111232", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111232", 
            "name": "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A9"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111232", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111232", 
            "name": "Walker-Warburg syndrome or muscle-eye-brain disease DAG1-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111232", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111232", 
            "name": "MDDGA9"
        }, 
        {
            "url": "https://www.omim.org/entry/616538", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616538", 
            "name": "Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A9"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111232", 
        "description": "A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in DAG1 on 3p21.31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111232", 
        "name": "congenital muscular dystrophy-dystroglycanopathy type A9"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616538", 
            "id": "616538", 
            "database": "MIM"
        }
    ]
}