{
    "disease_id": "DOID:0080281",
    "recommended_name": {
        "id": "DOID:0080281",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080281",
        "name": "schizophrenia 19",
        "description": "A schizophrenia that has_material_basis_in heterozygous mutation in the RBM12 gene on chromosome 20q11."
    },
    "synonyms": [
        {
            "id": "MONDO:0033312",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033312",
            "name": "schizophrenia 19",
            "description": ""
        },
        {
            "id": "MONDO:0033312",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033312",
            "name": "SCZD19",
            "description": ""
        },
        {
            "id": "MONDO:0033312",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033312",
            "name": "schizophrenia 19; SCZD19",
            "description": ""
        },
        {
            "id": "MONDO:0033312",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0033312",
            "name": "schizophrenia 19 with or without an affective disorder",
            "description": ""
        },
        {
            "id": "MIM:617629",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617629",
            "name": "Schizophrenia 19",
            "description": "Schizophrenia 19"
        }
    ]
}