{
    "disease_id": "DOID:0112169", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0112169", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112169", 
            "name": "NS11"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112169", 
        "description": "A Noonan syndrome characterized by clinical characteristics of Noonan syndrome, varying impairment of intellectual development, and cardiac hypertrophy that has_material_basis_in heterozygous mutation in MRAS on chromosome 3q22.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112169", 
        "name": "Noonan syndrome 11"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618499", 
            "id": "618499", 
            "database": "MIM"
        }
    ]
}