{
    "disease_id": "DOID:0110870", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010690", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010690", 
            "name": "nyctalopia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010690", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010690", 
            "name": "CSNB1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010690", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010690", 
            "name": "hemeralopia-myopia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010690", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010690", 
            "name": "NYX congenital stationary night blindness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010690", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010690", 
            "name": "congenital stationary night blindness caused by mutation in NYX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010690", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010690", 
            "name": "myopia-night blindness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010690", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010690", 
            "name": "congenital stationary night blindness with myopia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010690", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010690", 
            "name": "complete CSNB X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010690", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010690", 
            "name": "night blindness, congenital stationary, type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010690", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010690", 
            "name": "congenital stationary night blindness 1A X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010690", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010690", 
            "name": "congenital stationary night blindness type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010690", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010690", 
            "name": "night blindness, congenital stationary, type 1A; CSNB1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010690", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010690", 
            "name": "NBMI"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010690", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010690", 
            "name": "Csnb, complete, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010690", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010690", 
            "name": "night blindness, congenital stationary, with myopia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110870", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110870", 
            "name": "CSNB1A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110870", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110870", 
            "name": "NBMI"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110870", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110870", 
            "name": "complete CSNB X-linked"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110870", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110870", 
            "name": "congenital stationary night blindness 1A X-linked"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110870", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110870", 
            "name": "congenital stationary night blindness with myopia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110870", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110870", 
            "name": "hemeralopia-myopia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110870", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110870", 
            "name": "myopia-night blindness"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110870", 
        "description": "A congenital stationary night blindness that has_material_basis_in mutation in the NYX gene on chromosome Xp11.4.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110870", 
        "name": "congenital stationary night blindness 1A"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110870#disease-associations", 
            "id": "0110870", 
            "database": "Alliance of Genome Resources"
        }
    ]
}