{
    "disease_id": "DOID:0050559", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009678", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4; MDDGA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009678", 
            "name": "Walker-Warburg syndrome or muscle-eye-brain disease, Fktn-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009678", 
            "name": "FCMD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009678", 
            "name": "congenital muscular dystrophy, Fukuyama type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009678", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009678", 
            "name": "MDDGA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009678", 
            "name": "muscular dystrophy-dystroglycanopathy (Congenital with Brain and eye anomalies) type A, 4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050559", 
        "description": "A congenital muscular dystrophy-dystroglycanopathy type A that is characterized by muscle weakness, failure to thrive, severe intellectual and developmental disability, impaired vision and cardiac abnormalities and has_material_basis_in mutation in the FKTN gene that produces the fukutin protein.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050559", 
        "name": "Fukuyama congenital muscular dystrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050559#disease-associations", 
            "id": "0050559", 
            "database": "Alliance of Genome Resources"
        }
    ]
}