{
    "disease_id": "DOID:0061239",
    "recommended_name": {
        "id": "DOID:0061239",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061239",
        "name": "Stargardt disease 4",
        "description": "A stargardt disease that is characterized by decreased central vision, atrophy of the macula and underlying retinal pigment epithelium, and frequent presence of prominent flecks in the posterior pole of the retina and has_material_basis_in heterozygous mutation in the prominin-1 gene on chromosome 4p15."
    },
    "synonyms": [
        {
            "id": "MONDO:0011370",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011370",
            "name": "Stargardt disease 4",
            "description": "Any Stargardt disease in which the cause of the disease is a mutation in the PROM1 gene."
        },
        {
            "id": "MONDO:0011370",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011370",
            "name": "PROM1 Stargardt disease",
            "description": ""
        },
        {
            "id": "MONDO:0011370",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011370",
            "name": "Stargardt disease 4",
            "description": ""
        },
        {
            "id": "MONDO:0011370",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011370",
            "name": "Stargardt disease caused by mutation in PROM1",
            "description": ""
        },
        {
            "id": "MONDO:0011370",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011370",
            "name": "Stargardt disease type 4",
            "description": ""
        },
        {
            "id": "MONDO:0011370",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011370",
            "name": "STGD4",
            "description": ""
        },
        {
            "id": "MIM:603786",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/603786",
            "name": "Stargardt disease 4",
            "description": "Stargardt disease 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061239"
    ],
    "unlinked_id_list": []
}