{
    "disease_id": "DOID:0111230", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014071", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014071", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014071", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014071", 
            "name": "muscular dystrophy-dystroglycanopathy, type A caused by mutation in B3GALNT2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014071", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014071", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 11; MDDGA11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014071", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014071", 
            "name": "Walker-Warburg syndrome or muscle-eye-brain disease, B3Galnt2-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014071", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014071", 
            "name": "B3GALNT2 muscular dystrophy-dystroglycanopathy, type A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014071", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014071", 
            "name": "MDDGA11"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111230", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111230", 
            "name": "MDDGA11"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111230", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111230", 
            "name": "Walker-Warburg syndrome or muscle-eye-brain disease B3GALNT2-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111230", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111230", 
            "name": "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A11"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111230", 
        "description": "A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in B3GALNT2 on 1q42.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111230", 
        "name": "congenital muscular dystrophy-dystroglycanopathy type A11"
    }, 
    "evidence": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014071", 
            "id": "0014071", 
            "database": "MONDO"
        }, 
        {
            "url": "https://www.omim.org/entry/615181", 
            "id": "615181", 
            "database": "MIM"
        }
    ]
}