{
    "disease_id": "DOID:0111229", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009364", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009364", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009364", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009364", 
            "name": "hard syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009364", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009364", 
            "name": "Walker-Warburg syndrome or muscle-eye-brain disease, Pomt1-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009364", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009364", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009364", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009364", 
            "name": "cod-MD syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009364", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009364", 
            "name": "MDDGA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009364", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009364", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009364", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009364", 
            "name": "cerebroocular dysplasia-muscular dystrophy syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009364", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009364", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1; MDDGA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009364", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009364", 
            "name": "hydrocephalus, agyria, and retinal dysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111229", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111229", 
            "name": "klissencephaly type 2 with muscular and ocular involvement"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111229", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111229", 
            "name": "MDDGA"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111229", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111229", 
            "name": "congenital muscular alpha-dystroglycanopathy with brain and eye anomalies"
        }, 
        {
            "url": "https://www.omim.org/entry/236670", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:236670", 
            "name": "Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111229", 
        "description": "A congenital muscular dystrophy-dystroglycanopathy type A characterized by cobblestone lissencephaly, muscle weakness, and brain and eye anomalies that has_material_basis_in autosomal recessive inheritance a defect in alpha-dystroglycan post-translational processing.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111229", 
        "name": "congenital muscular dystrophy-dystroglycanopathy type A"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/236670", 
            "id": "236670", 
            "database": "MIM"
        }
    ]
}