{
    "disease_id": "DOID:0110862",
    "recommended_name": {
        "id": "DOID:0110862",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110862",
        "name": "congenital stationary night blindness autosomal dominant 1",
        "description": "A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in mutations in the RHO gene on chromosome 3q22.1."
    },
    "synonyms": [
        {
            "id": "DOID:0110862",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110862",
            "name": "rhodopsin-related congenital stationary night blindness",
            "description": ""
        },
        {
            "id": "DOID:0110862",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110862",
            "name": "CSNBAD1",
            "description": ""
        },
        {
            "id": "MONDO:0012498",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012498",
            "name": "congenital stationary night blindness autosomal dominant 1",
            "description": "Any congenital stationary night blindness in which the cause of the disease is a mutation in the RHO gene."
        },
        {
            "id": "MONDO:0012498",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012498",
            "name": "CSNBAD1",
            "description": ""
        },
        {
            "id": "MONDO:0012498",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012498",
            "name": "RHO congenital stationary night blindness",
            "description": ""
        },
        {
            "id": "MONDO:0012498",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012498",
            "name": "congenital stationary night blindness autosomal dominant type 1",
            "description": ""
        },
        {
            "id": "MONDO:0012498",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012498",
            "name": "congenital stationary night blindness caused by mutation in RHO",
            "description": ""
        },
        {
            "id": "MONDO:0012498",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012498",
            "name": "night blindness, congenital stationary, autosomal dominant type 1",
            "description": ""
        },
        {
            "id": "MONDO:0012498",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012498",
            "name": "rhodopsin-related congenital stationary night blindness",
            "description": ""
        },
        {
            "id": "MONDO:0012498",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012498",
            "name": "night blindness, congenital stationary, autosomal dominant 1",
            "description": ""
        },
        {
            "id": "MONDO:0012498",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012498",
            "name": "night blindness, congenital stationary, rhodopsin-related",
            "description": ""
        },
        {
            "id": "MIM:610445",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/610445",
            "name": "Night blindness, congenital stationary, autosomal dominant 1",
            "description": "Night blindness, congenital stationary, autosomal dominant 1"
        }
    ]
}