{
    "disease_id": "DOID:0110008",
    "recommended_name": {
        "id": "DOID:0110008",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110008",
        "name": "achromatopsia 3",
        "description": "An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGB3 gene on chromosome 8q2."
    },
    "synonyms": [
        {
            "id": "DOID:0110008",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110008",
            "name": "ACHM1",
            "description": ""
        },
        {
            "id": "DOID:0110008",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110008",
            "name": "ACHM3",
            "description": ""
        },
        {
            "id": "DOID:0110008",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110008",
            "name": "Pingelapese blindness",
            "description": ""
        },
        {
            "id": "DOID:0110008",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110008",
            "name": "RMCH1",
            "description": ""
        },
        {
            "id": "DOID:0110008",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110008",
            "name": "rod monochromacy 1",
            "description": ""
        },
        {
            "id": "DOID:0110008",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110008",
            "name": "rod monochromatism 1",
            "description": ""
        },
        {
            "id": "MONDO:0009875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009875",
            "name": "achromatopsia 3",
            "description": "Any achromatopsia in which the cause of the disease is a mutation in the CNGB3 gene."
        },
        {
            "id": "MONDO:0009875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009875",
            "name": "ACHM3",
            "description": ""
        },
        {
            "id": "MONDO:0009875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009875",
            "name": "CNGB3 achromatopsia",
            "description": ""
        },
        {
            "id": "MONDO:0009875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009875",
            "name": "achromatopsia 3",
            "description": ""
        },
        {
            "id": "MONDO:0009875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009875",
            "name": "achromatopsia caused by mutation in CNGB3",
            "description": ""
        },
        {
            "id": "MONDO:0009875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009875",
            "name": "achromatopsia type 3",
            "description": ""
        },
        {
            "id": "MONDO:0009875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009875",
            "name": "ACHM1 (formerly)",
            "description": ""
        },
        {
            "id": "MONDO:0009875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009875",
            "name": "RMCH1 (formerly)",
            "description": ""
        },
        {
            "id": "MONDO:0009875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009875",
            "name": "Rod monochromacy 1 (formerly)",
            "description": ""
        },
        {
            "id": "MONDO:0009875",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009875",
            "name": "Rod monochromatism 1 (formerly)",
            "description": ""
        },
        {
            "id": "MIM:262300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/262300",
            "name": "Achromatopsia 3",
            "description": "Achromatopsia 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110008"
    ],
    "unlinked_id_list": []
}