{
    "disease_id": "DOID:0070364",
    "recommended_name": {
        "id": "DOID:0070364",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070364",
        "name": "bradyopsia 2",
        "description": "A braydopsia that has_material_basis_in homozygous mutation in the RGS9BP gene on chromosome 19q13."
    },
    "synonyms": [
        {
            "id": "DOID:0070364",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070364",
            "name": "prolonged electroretinal response suppression 2",
            "description": ""
        },
        {
            "id": "MONDO:0958190",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0958190",
            "name": "prolonged electroretinal response suppression 2",
            "description": ""
        },
        {
            "id": "MIM:620344",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620344",
            "name": "Prolonged electroretinal response suppression 2",
            "description": "Prolonged electroretinal response suppression 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070364"
    ],
    "unlinked_id_list": []
}