{
    "disease_id": "DOID:0110010",
    "recommended_name": {
        "id": "DOID:0110010",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110010",
        "name": "achromatopsia 4",
        "description": "An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the GNAT2 gene on chromosome 1p13."
    },
    "synonyms": [
        {
            "id": "DOID:0110010",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110010",
            "name": "ACHM4",
            "description": ""
        },
        {
            "id": "MONDO:0013465",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013465",
            "name": "achromatopsia 4",
            "description": "Any achromatopsia in which the cause of the disease is a mutation in the GNAT2 gene."
        },
        {
            "id": "MONDO:0013465",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013465",
            "name": "ACHM4",
            "description": ""
        },
        {
            "id": "MONDO:0013465",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013465",
            "name": "GNAT2 achromatopsia",
            "description": ""
        },
        {
            "id": "MONDO:0013465",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013465",
            "name": "achromatopsia 4",
            "description": ""
        },
        {
            "id": "MONDO:0013465",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013465",
            "name": "achromatopsia caused by mutation in GNAT2",
            "description": ""
        },
        {
            "id": "MONDO:0013465",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013465",
            "name": "achromatopsia type 4",
            "description": ""
        },
        {
            "id": "MIM:613856",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613856",
            "name": "Achromatopsia 4",
            "description": "Achromatopsia 4"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110010"
    ],
    "unlinked_id_list": []
}