{
    "disease_id": "DOID:0110261",
    "recommended_name": {
        "id": "DOID:0110261",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0110261",
        "name": "cataract 35",
        "description": "A cataract that has_material_basis_in variation in the region 19q13."
    },
    "synonyms": [
        {
            "id": "DOID:0110261",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110261",
            "name": "CATCN1",
            "description": ""
        },
        {
            "id": "DOID:0110261",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110261",
            "name": "CTRCT35",
            "description": ""
        },
        {
            "id": "DOID:0110261",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110261",
            "name": "autosomal recessive congenital nuclear cataract 1",
            "description": ""
        },
        {
            "id": "DOID:0110261",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0110261",
            "name": "cataract 35, congenital nuclear",
            "description": ""
        },
        {
            "id": "MONDO:0012260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012260",
            "name": "cataract 35",
            "description": "A cataract that has material basis in variation in the region 19q13."
        },
        {
            "id": "MONDO:0012260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012260",
            "name": "CATCN1",
            "description": ""
        },
        {
            "id": "MONDO:0012260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012260",
            "name": "CTRCT35",
            "description": ""
        },
        {
            "id": "MONDO:0012260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012260",
            "name": "autosomal recessive congenital nuclear cataract 1",
            "description": ""
        },
        {
            "id": "MONDO:0012260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012260",
            "name": "cataract 35",
            "description": ""
        },
        {
            "id": "MONDO:0012260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012260",
            "name": "cataract 35, congenital nuclear",
            "description": ""
        },
        {
            "id": "MONDO:0012260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012260",
            "name": "cataract type 35",
            "description": ""
        },
        {
            "id": "MONDO:0012260",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012260",
            "name": "cataract, congenital nuclear, autosomal recessive 1",
            "description": ""
        }
    ]
}