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