{
    "disease_id": "DOID:0110862", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012498", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012498", 
            "name": "night blindness, congenital stationary, autosomal dominant type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012498", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012498", 
            "name": "RHO congenital stationary night blindness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012498", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012498", 
            "name": "congenital stationary night blindness caused by mutation in RHO"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012498", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012498", 
            "name": "night blindness, congenital stationary, rhodopsin-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012498", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012498", 
            "name": "rhodopsin-related congenital stationary night blindness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012498", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012498", 
            "name": "night blindness, congenital stationary, autosomal dominant 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012498", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012498", 
            "name": "congenital stationary night blindness autosomal dominant type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012498", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012498", 
            "name": "CSNBAD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012498", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012498", 
            "name": "night blindness, congenital stationary, autosomal dominant 1; CSNBAD1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110862", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110862", 
            "name": "rhodopsin-related congenital stationary night blindness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110862", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110862", 
            "name": "CSNBAD1"
        }, 
        {
            "url": "https://www.omim.org/entry/610445", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:610445", 
            "name": "Night blindness, congenital stationary, autosomal dominant 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110862", 
        "description": "A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in mutations in the RHO gene on chromosome 3q22.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110862", 
        "name": "congenital stationary night blindness autosomal dominant 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/610445", 
            "id": "610445", 
            "database": "MIM"
        }
    ]
}