{
    "disease_id": "DOID:0070089",
    "recommended_name": {
        "id": "DOID:0070089",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070089",
        "name": "schizophrenia 13",
        "description": "A schizophrenia that has_material_basis_in a mutation on chromosome 15q13."
    },
    "synonyms": [
        {
            "id": "DOID:0070089",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070089",
            "name": "SCZD13",
            "description": ""
        },
        {
            "id": "MONDO:0013089",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013089",
            "name": "schizophrenia 13",
            "description": "A schizophrenia that has material basis in a mutation on chromosome 15q13."
        },
        {
            "id": "MONDO:0013089",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013089",
            "name": "SCZD13",
            "description": ""
        },
        {
            "id": "MONDO:0013089",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013089",
            "name": "schizophrenia 13",
            "description": ""
        },
        {
            "id": "MONDO:0013089",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013089",
            "name": "schizophrenia susceptibility locus, chromosome 15Q13-q14-related",
            "description": ""
        },
        {
            "id": "MONDO:0013089",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013089",
            "name": "schizophrenia, susceptibility to, 13",
            "description": ""
        },
        {
            "id": "MONDO:0013089",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013089",
            "name": "schizophrenia, Neurophysiologic defect 1N",
            "description": ""
        }
    ]
}