{
    "disease_id": "DOID:0110242",
    "recommended_name": {
        "id": "DOID:0110242",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110242",
        "name": "cataract 13 with adult i phenotype",
        "description": "A cataract that has_material_basis_in homozygous or compound heterozygous mutation in the GCNT2 gene on chromosome 6p24."
    },
    "synonyms": [
        {
            "id": "DOID:0110242",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110242",
            "name": "CTRCT13",
            "description": ""
        },
        {
            "id": "MONDO:0007289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007289",
            "name": "cataract 13 with adult I phenotype",
            "description": "A cataract that has material basis in homozygous or compound heterozygous mutation in the GCNT2 gene on chromosome 6p24."
        },
        {
            "id": "MONDO:0007289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007289",
            "name": "CTRCT13",
            "description": ""
        },
        {
            "id": "MONDO:0007289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007289",
            "name": "cataract 13 with adult I phenotype",
            "description": ""
        },
        {
            "id": "MIM:116700",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/116700",
            "name": "Cataract 13, with adult i phenotype",
            "description": "Cataract 13, with adult i phenotype"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110242"
    ],
    "unlinked_id_list": []
}