{
    "disease_id": "DOID:0112169",
    "recommended_name": {
        "id": "DOID:0112169",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112169",
        "name": "Noonan syndrome 11",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0112169",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112169",
            "name": "NS11",
            "description": ""
        },
        {
            "id": "MIM:618499",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618499",
            "name": "Noonan syndrome 11",
            "description": "Noonan syndrome 11"
        }
    ]
}