{
    "disease_id": "DOID:0070354",
    "recommended_name": {
        "id": "DOID:0070354",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070354",
        "name": "cataract 48",
        "description": "A cataract that has_material_basis_in homozygous mutation in the DNMBP gene on chromosome 10q24 and is characterized by infantile or early-childhood cataracts and visual impairment."
    },
    "synonyms": [
        {
            "id": "DOID:0070354",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070354",
            "name": "CTRCT48",
            "description": ""
        },
        {
            "id": "MONDO:0032735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032735",
            "name": "cataract 48",
            "description": ""
        },
        {
            "id": "MONDO:0032735",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032735",
            "name": "CTRCT48",
            "description": ""
        },
        {
            "id": "MIM:618415",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618415",
            "name": "Cataract 48",
            "description": "Cataract 48"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070354"
    ],
    "unlinked_id_list": []
}