{
    "disease_id": "DOID:0050736", 
    "synonyms": [], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050736", 
        "description": "An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050736", 
        "name": "autosomal dominant disease"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050736#disease-associations", 
            "id": "0050736", 
            "database": "Alliance of Genome Resources"
        }
    ]
}