{
    "disease_id": "DOID:0111241",
    "recommended_name": {
        "id": "DOID:0111241",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111241",
        "name": "congenital muscular dystrophy-dystroglycanopathy type A5",
        "description": "A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in FKRP on 19q13.32."
    },
    "synonyms": [
        {
            "id": "DOID:0111241",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111241",
            "name": "congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5",
            "description": ""
        },
        {
            "id": "DOID:0111241",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111241",
            "name": "MDDGA5",
            "description": ""
        },
        {
            "id": "DOID:0111241",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111241",
            "name": "Walker-Warburg syndrome or muscle-eye-brain disease, FKRP-related",
            "description": ""
        },
        {
            "id": "MONDO:0013157",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013157",
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5",
            "description": ""
        },
        {
            "id": "MONDO:0013157",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013157",
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5",
            "description": ""
        },
        {
            "id": "MONDO:0013157",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013157",
            "name": "MDDGA5",
            "description": ""
        },
        {
            "id": "MONDO:0013157",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013157",
            "name": "Walker-Warburg syndrome or muscle-eye-brain disease, FKRP-related",
            "description": ""
        },
        {
            "id": "MONDO:0013157",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013157",
            "name": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5; MDDGA5",
            "description": ""
        },
        {
            "id": "MIM:613153",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613153",
            "name": "Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A5",
            "description": "Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A5"
        }
    ]
}