{
    "disease_id": "DOID:0111233", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111233", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111233", 
            "name": "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A14"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111233", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111233", 
            "name": "MDDGA14"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111233", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111233", 
            "name": "Walker-Warburg syndrome or muscle-eye-brain disease GMPPB-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014140", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014140", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014140", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014140", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14; MDDGA14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014140", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014140", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014140", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014140", 
            "name": "MDDGA14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014140", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014140", 
            "name": "Walker-Warburg syndrome or muscle-eye-brain disease, GMPPB-related"
        }, 
        {
            "url": "https://www.omim.org/entry/615350", 
            "description": "Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A14", 
            "resource": "MIM", 
            "id": "MIM:615350", 
            "name": "Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A14"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111233", 
        "description": "A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in in GMPPB on 3p21.31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111233", 
        "name": "congenital muscular dystrophy-dystroglycanopathy A14"
    }
}