{
    "disease_id": "DOID:0110864",
    "recommended_name": {
        "id": "DOID:0110864",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110864",
        "name": "congenital stationary night blindness 1F",
        "description": "A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in compound heterozygous mutation in the LRIT3 gene on chromosome 4q25."
    },
    "synonyms": [
        {
            "id": "DOID:0110864",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110864",
            "name": "CSNB1F",
            "description": ""
        },
        {
            "id": "DOID:0110864",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110864",
            "name": "congenital stationary night blindness 1F autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0014026",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014026",
            "name": "congenital stationary night blindness 1F",
            "description": "Any congenital stationary night blindness in which the cause of the disease is a mutation in the LRIT3 gene."
        },
        {
            "id": "MONDO:0014026",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014026",
            "name": "CSNB1F",
            "description": ""
        },
        {
            "id": "MONDO:0014026",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014026",
            "name": "LRIT3 congenital stationary night blindness",
            "description": ""
        },
        {
            "id": "MONDO:0014026",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014026",
            "name": "congenital stationary night blindness caused by mutation in LRIT3",
            "description": ""
        },
        {
            "id": "MONDO:0014026",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014026",
            "name": "congenital stationary night blindness type 1F",
            "description": ""
        },
        {
            "id": "MONDO:0014026",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014026",
            "name": "night blindness, congenital stationary (complete), 1F, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0014026",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014026",
            "name": "night blindness, congenital stationary, type 1F",
            "description": ""
        },
        {
            "id": "MIM:615058",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615058",
            "name": "Night blindness, congenital stationary, 1F",
            "description": "Night blindness, congenital stationary, 1F"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110864"
    ],
    "unlinked_id_list": []
}