{
    "disease_id": "DOID:0110863",
    "recommended_name": {
        "id": "DOID:0110863",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110863",
        "name": "congenital stationary night blindness autosomal dominant 2",
        "description": "A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the PDE6B gene on chromosome 4p16."
    },
    "synonyms": [
        {
            "id": "DOID:0110863",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110863",
            "name": "CSNBAD2",
            "description": ""
        },
        {
            "id": "DOID:0110863",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110863",
            "name": "Rambusch type congenital stationary night blindness",
            "description": ""
        },
        {
            "id": "MONDO:0008099",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008099",
            "name": "congenital stationary night blindness autosomal dominant 2",
            "description": "Any congenital stationary night blindness in which the cause of the disease is a mutation in the PDE6B gene."
        },
        {
            "id": "MONDO:0008099",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008099",
            "name": "CSNBAD2",
            "description": ""
        },
        {
            "id": "MONDO:0008099",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008099",
            "name": "PDE6B congenital stationary night blindness",
            "description": ""
        },
        {
            "id": "MONDO:0008099",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008099",
            "name": "congenital stationary night blindness autosomal dominant type 2",
            "description": ""
        },
        {
            "id": "MONDO:0008099",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008099",
            "name": "congenital stationary night blindness caused by mutation in PDE6B",
            "description": ""
        },
        {
            "id": "MONDO:0008099",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008099",
            "name": "night blindness, congenital stationary, autosomal dominant type 2",
            "description": ""
        },
        {
            "id": "MONDO:0008099",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008099",
            "name": "night blindness, congenital stationary, autosomal dominant 2",
            "description": ""
        },
        {
            "id": "MIM:163500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/163500",
            "name": "Night blindness, congenital stationary, autosomal dominant 2",
            "description": "Night blindness, congenital stationary, autosomal dominant 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110863"
    ],
    "unlinked_id_list": []
}