{
    "disease_id": "DOID:0110715",
    "recommended_name": {
        "id": "DOID:0110715",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110715",
        "name": "congenital stationary night blindness autosomal dominant 3",
        "description": "A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the GNAT1 gene on chromosome 3p21."
    },
    "synonyms": [
        {
            "id": "DOID:0110715",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110715",
            "name": "CSNBAD3",
            "description": ""
        },
        {
            "id": "DOID:0110715",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110715",
            "name": "Nougaret type congenital stationary night blindness",
            "description": ""
        },
        {
            "id": "MONDO:0012497",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012497",
            "name": "congenital stationary night blindness autosomal dominant 3",
            "description": "A congenital stationary night blindness characterized by autosomal dominant inheritance that has material basis in heterozygous mutation in the GNAT1 gene on chromosome 3p21."
        },
        {
            "id": "MONDO:0012497",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012497",
            "name": "CSNBAD3",
            "description": ""
        },
        {
            "id": "MONDO:0012497",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012497",
            "name": "congenital stationary night blindness autosomal dominant type 3",
            "description": ""
        },
        {
            "id": "MONDO:0012497",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012497",
            "name": "night blindness, congenital stationary, autosomal dominant type 3",
            "description": ""
        },
        {
            "id": "MONDO:0012497",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012497",
            "name": "night blindness, congenital stationary, autosomal dominant 3",
            "description": ""
        },
        {
            "id": "MIM:610444",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/610444",
            "name": "Night blindness, congenital stationary, autosomal dominant 3",
            "description": "Night blindness, congenital stationary, autosomal dominant 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110715"
    ],
    "unlinked_id_list": []
}