{
    "disease_id": "DOID:0110866",
    "recommended_name": {
        "id": "DOID:0110866",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110866",
        "name": "congenital stationary night blindness 1H",
        "description": "A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in homozygous or compound heterozygous mutation in the GNB3 gene on chromosome 12p13."
    },
    "synonyms": [
        {
            "id": "DOID:0110866",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110866",
            "name": "CSNB1H",
            "description": ""
        },
        {
            "id": "DOID:0110866",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110866",
            "name": "congenital stationary night blindness type 1H",
            "description": ""
        },
        {
            "id": "MONDO:0014872",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014872",
            "name": "congenital stationary night blindness 1H",
            "description": "Any congenital stationary night blindness in which the cause of the disease is a mutation in the GNB3 gene."
        },
        {
            "id": "MONDO:0014872",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014872",
            "name": "GNB3 congenital stationary night blindness",
            "description": ""
        },
        {
            "id": "MONDO:0014872",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014872",
            "name": "night blindness, congenital stationary, type 1H",
            "description": ""
        },
        {
            "id": "MONDO:0014872",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014872",
            "name": "congenital stationary night blindness type 1H",
            "description": ""
        },
        {
            "id": "MONDO:0014872",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014872",
            "name": "night blindness, congenital stationary, type 1H; CSNB1H",
            "description": ""
        },
        {
            "id": "MONDO:0014872",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014872",
            "name": "congenital stationary night blindness caused by mutation in GNB3",
            "description": ""
        },
        {
            "id": "MONDO:0014872",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014872",
            "name": "CSNB1H",
            "description": ""
        },
        {
            "id": "MIM:617024",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617024",
            "name": "Night blindness, congenital stationary, 1H",
            "description": "Night blindness, congenital stationary, 1H"
        }
    ]
}