{
    "disease_id": "DOID:0050534",
    "recommended_name": {
        "id": "DOID:0050534",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050534",
        "name": "congenital stationary night blindness",
        "description": "A hereditary night blindness that is characterized by hemeralopia with a moderate loss of visual acuity and caused by defective photoreceptor-to-bipolar cell signaling with common ERG findings of reduced or absent b-waves and generally normal a-waves."
    },
    "synonyms": [
        {
            "id": "DOID:0050534",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050534",
            "name": "congenital essential nyctalopia",
            "description": ""
        },
        {
            "id": "MONDO:0010690",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010690",
            "name": "congenital stationary night blindness 1A",
            "description": "A congenital stationary night blindness caused by variants in the X-linked NYX gene."
        },
        {
            "id": "MONDO:0010690",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010690",
            "name": "CSNB1A",
            "description": ""
        },
        {
            "id": "MONDO:0010690",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010690",
            "name": "NYX congenital stationary night blindness",
            "description": ""
        },
        {
            "id": "MONDO:0010690",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010690",
            "name": "NYX-related congenital stationary night blindness",
            "description": ""
        },
        {
            "id": "MONDO:0010690",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010690",
            "name": "congenital stationary night blindness caused by mutation in NYX",
            "description": ""
        },
        {
            "id": "MONDO:0010690",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010690",
            "name": "congenital stationary night blindness type 1A",
            "description": ""
        },
        {
            "id": "MONDO:0010690",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010690",
            "name": "hemeralopia-myopia",
            "description": ""
        },
        {
            "id": "MONDO:0010690",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010690",
            "name": "myopia-night blindness",
            "description": ""
        },
        {
            "id": "MONDO:0010690",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010690",
            "name": "night blindness, congenital stationary (complete), 1A, X-linked, X-linked recessive",
            "description": ""
        },
        {
            "id": "MONDO:0010690",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010690",
            "name": "night blindness, congenital stationary, type 1A",
            "description": ""
        },
        {
            "id": "MIM:310500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/310500",
            "name": "Night blindness, congenital stationary, 1A",
            "description": "Night blindness, congenital stationary, 1A"
        }
    ],
    "children": [
        {
            "id": "DOID:0110712",
            "label": "Oguchi disease-1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110713",
            "label": "Oguchi disease-2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110714",
            "label": "congenital stationary night blindness 1G",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110715",
            "label": "congenital stationary night blindness autosomal dominant 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110862",
            "label": "congenital stationary night blindness autosomal dominant 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110863",
            "label": "congenital stationary night blindness autosomal dominant 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110864",
            "label": "congenital stationary night blindness 1F",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110865",
            "label": "congenital stationary night blindness 1B",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110866",
            "label": "congenital stationary night blindness 1H",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110867",
            "label": "congenital stationary night blindness 1C",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110868",
            "label": "congenital stationary night blindness 1D",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110869",
            "label": "congenital stationary night blindness 1E",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110870",
            "label": "congenital stationary night blindness 1A",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0110871",
            "label": "congenital stationary night blindness 2A",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0110713",
        "DOID:0110866",
        "DOID:0050534",
        "DOID:0110864",
        "DOID:0110869",
        "DOID:0110862",
        "DOID:0110715",
        "DOID:0110865",
        "DOID:0110868",
        "DOID:0110867",
        "DOID:0110712",
        "DOID:0110871",
        "DOID:0110870",
        "DOID:0110863",
        "DOID:0110714"
    ],
    "unlinked_id_list": []
}