{
    "disease_id": "DOID:0110260", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007279", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007279", 
            "name": "CCA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007279", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007279", 
            "name": "cataract type 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007279", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007279", 
            "name": "cataract, congenital, cerulean type, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007279", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007279", 
            "name": "congenital cerulean type cataract 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007279", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007279", 
            "name": "cataract 7; CTRCT7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007279", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007279", 
            "name": "CTRCT7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007279", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007279", 
            "name": "cerulean type cataract 7"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007279", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007279", 
            "name": "cataract 7, cerulean type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110260", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110260", 
            "name": "CTRCT7"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110260", 
        "description": "A cataract that has_material_basis_in variation in the region 17q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110260", 
        "name": "cataract 7"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110260#disease-associations", 
            "id": "0110260", 
            "database": "Alliance of Genome Resources"
        }
    ]
}