{
    "disease_id": "DOID:0110233", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011808", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011808", 
            "name": "cataract type 27"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011808", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011808", 
            "name": "cataract 27; CTRCT27"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011808", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011808", 
            "name": "CTRCT27"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011808", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011808", 
            "name": "cataract 27 nuclear progressive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011808", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011808", 
            "name": "cataract 27, nuclear progressive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011808", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011808", 
            "name": "Ccnp"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110233", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110233", 
            "name": "CTRCT27"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110233", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110233", 
            "name": "cataract 27 nuclear progressive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110233", 
        "description": "A cataract that has_material_basis_in mutation in the region 2p12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110233", 
        "name": "cataract 27"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110233#disease-associations", 
            "id": "0110233", 
            "database": "Alliance of Genome Resources"
        }
    ]
}