{
    "disease_id": "DOID:0110870",
    "recommended_name": {
        "id": "DOID:0110870",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110870",
        "name": "congenital stationary night blindness 1A",
        "description": "A congenital stationary night blindness that has_material_basis_in mutation in the NYX gene on chromosome Xp11.4."
    },
    "synonyms": [
        {
            "id": "DOID:0110870",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110870",
            "name": "CSNB1A",
            "description": ""
        },
        {
            "id": "DOID:0110870",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110870",
            "name": "NBMI",
            "description": ""
        },
        {
            "id": "DOID:0110870",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110870",
            "name": "complete CSNB X-linked",
            "description": ""
        },
        {
            "id": "DOID:0110870",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110870",
            "name": "congenital stationary night blindness 1A X-linked",
            "description": ""
        },
        {
            "id": "DOID:0110870",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110870",
            "name": "congenital stationary night blindness with myopia",
            "description": ""
        },
        {
            "id": "DOID:0110870",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110870",
            "name": "hemeralopia-myopia",
            "description": ""
        },
        {
            "id": "DOID:0110870",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110870",
            "name": "myopia-night blindness",
            "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_list": [
        "DOID:0110870"
    ],
    "unlinked_id_list": []
}