{
    "disease_id": "DOID:0111411",
    "recommended_name": {
        "id": "DOID:0111411",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111411",
        "name": "exudative vitreoretinopathy 4",
        "description": "An exudative vitreoretinopathy that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the LRP5 gene on chromosome 11q13.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111411",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111411",
            "name": "EVR4",
            "description": ""
        },
        {
            "id": "MONDO:0011151",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011151",
            "name": "exudative vitreoretinopathy 4",
            "description": ""
        },
        {
            "id": "MONDO:0011151",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011151",
            "name": "exudative vitreoretinopathy 4",
            "description": ""
        },
        {
            "id": "MONDO:0011151",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011151",
            "name": "exudative vitreoretinopathy type 4",
            "description": ""
        },
        {
            "id": "MONDO:0011151",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011151",
            "name": "EVR4",
            "description": ""
        },
        {
            "id": "MIM:601813",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/601813",
            "name": "Vitreoretinopathy, exudative 4",
            "description": "Vitreoretinopathy, exudative 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111411"
    ],
    "unlinked_id_list": []
}