{
    "disease_id": "DOID:0111240", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013154", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013154", 
            "name": "MDDGA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013154", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013154", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2; MDDGA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013154", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013154", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013154", 
            "name": "Walker-Warburg syndrome or muscle-eye-brain disease, Pomt2-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111240", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111240", 
            "name": "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111240", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111240", 
            "name": "MDDGA2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111240", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111240", 
            "name": "Walker-Warburg syndrome or muscle-eye-brain disease, POMT2-related"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111240", 
        "description": "A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in POMT2 on 14q24.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111240", 
        "name": "congenital muscular dystrophy-dystroglycanopathy type A2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111240#disease-associations", 
            "id": "0111240", 
            "database": "Alliance of Genome Resources"
        }
    ]
}