{
    "disease_id": "DOID:0110238",
    "recommended_name": {
        "id": "DOID:0110238",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110238",
        "name": "cataract 18",
        "description": "A cataract that has_material_basis_in homozygous mutation in the FYCO1 gene on chromosome 3p21.3."
    },
    "synonyms": [
        {
            "id": "DOID:0110238",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110238",
            "name": "CATC2",
            "description": ""
        },
        {
            "id": "DOID:0110238",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110238",
            "name": "CTRCT18",
            "description": ""
        },
        {
            "id": "DOID:0110238",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110238",
            "name": "autosomal recessive congenital cataract 2",
            "description": ""
        },
        {
            "id": "DOID:0110238",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110238",
            "name": "cataract 18 autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0012395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012395",
            "name": "cataract 18",
            "description": "Any cataract in which the cause of the disease is a mutation in the FYCO1 gene."
        },
        {
            "id": "MONDO:0012395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012395",
            "name": "CATC2",
            "description": ""
        },
        {
            "id": "MONDO:0012395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012395",
            "name": "CTRCT18",
            "description": ""
        },
        {
            "id": "MONDO:0012395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012395",
            "name": "FYCO1 cataract (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0012395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012395",
            "name": "cataract (disease) caused by mutation in FYCO1",
            "description": ""
        },
        {
            "id": "MONDO:0012395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012395",
            "name": "cataract 18",
            "description": ""
        },
        {
            "id": "MONDO:0012395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012395",
            "name": "cataract 18, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0012395",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012395",
            "name": "cataract type 18",
            "description": ""
        },
        {
            "id": "MIM:610019",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/610019",
            "name": "Cataract 18",
            "description": "Cataract 18"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110238"
    ],
    "unlinked_id_list": []
}