{
    "disease_id": "DOID:0110871",
    "recommended_name": {
        "id": "DOID:0110871",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110871",
        "name": "congenital stationary night blindness 2A",
        "description": "A congenital stationary night blindness that has_material_basis_in mutation in the CACNA1F gene on chromosome Xp11.23."
    },
    "synonyms": [
        {
            "id": "DOID:0110871",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110871",
            "name": "congenital stationary night blindness 2A X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010241",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010241",
            "name": "congenital stationary night blindness 2A",
            "description": "Any congenital stationary night blindness in which the cause of the disease is a mutation in the CACNA1F gene."
        },
        {
            "id": "MONDO:0010241",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010241",
            "name": "CACNA1F congenital stationary night blindness",
            "description": ""
        },
        {
            "id": "MONDO:0010241",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010241",
            "name": "CSNB, incomplete, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010241",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010241",
            "name": "congenital stationary night blindness 2A X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010241",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010241",
            "name": "congenital stationary night blindness caused by mutation in CACNA1F",
            "description": ""
        },
        {
            "id": "MONDO:0010241",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010241",
            "name": "congenital stationary night blindness type 2A",
            "description": ""
        },
        {
            "id": "MONDO:0010241",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010241",
            "name": "night blindness, congenital stationary (incomplete), 2A, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010241",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010241",
            "name": "CSNB2A",
            "description": ""
        },
        {
            "id": "MONDO:0010241",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010241",
            "name": "night blindness, congenital stationary, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010241",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010241",
            "name": "night blindness, congenital stationary, type 2A",
            "description": ""
        },
        {
            "id": "MIM:300071",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300071",
            "name": "Night blindness, congenital stationary, 2A",
            "description": "Night blindness, congenital stationary, 2A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110871"
    ],
    "unlinked_id_list": []
}