{
    "disease_id": "DOID:0110236",
    "recommended_name": {
        "id": "DOID:0110236",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110236",
        "name": "cataract 39 multiple types",
        "description": "A cataract that has_material_basis_in heterozygous mutation in the CRYGB gene on chromosome 2q34."
    },
    "synonyms": [
        {
            "id": "DOID:0110236",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110236",
            "name": "CTRCT39",
            "description": ""
        },
        {
            "id": "DOID:0110236",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110236",
            "name": "autosomal dominant cataract 39 multiple types",
            "description": ""
        },
        {
            "id": "MONDO:0014075",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014075",
            "name": "cataract 39 multiple types",
            "description": "Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the CRYGB gene."
        },
        {
            "id": "MONDO:0014075",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014075",
            "name": "CRYGB early-onset non-syndromic cataract",
            "description": ""
        },
        {
            "id": "MONDO:0014075",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014075",
            "name": "CTRCT39",
            "description": ""
        },
        {
            "id": "MONDO:0014075",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014075",
            "name": "cataract 39, multiple types, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0014075",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014075",
            "name": "early-onset non-syndromic cataract caused by mutation in CRYGB",
            "description": ""
        },
        {
            "id": "MONDO:0014075",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014075",
            "name": "cataract 39, multiple types",
            "description": ""
        },
        {
            "id": "MIM:615188",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615188",
            "name": "Cataract 39, multiple types",
            "description": "Cataract 39, multiple types"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110236"
    ],
    "unlinked_id_list": []
}