{
    "disease_id": "DOID:0050560",
    "recommended_name": {
        "id": "DOID:0050560",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050560",
        "name": "Walker-Warburg syndrome",
        "description": "A congenital muscular dystrophy that is characterized by hypotonia, seizures, severe intellectual and developmental disability, eye abnormalities and early death and has_material_basis_in mutations in multiple genes including POMT1, POMT2, ISPD, FKTN, FKRP, and LARGE1."
    },
    "synonyms": [
        {
            "id": "DOID:0050560",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050560",
            "name": "HARD syndrome",
            "description": ""
        },
        {
            "id": "DOID:0050560",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050560",
            "name": "cerebroocular dysplasia-muscular dystrophy syndrome",
            "description": ""
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050560"
    ],
    "unlinked_id_list": []
}