{
    "disease_id": "DOID:0112170",
    "recommended_name": {
        "id": "DOID:0112170",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112170",
        "name": "Noonan syndrome 12",
        "description": "A Noonan syndrome characterized by macrocephaly, facial anomalies including hypertelorism, downslanting palpebral fissures, and low-set ears, and other Noonan syndrome features that has_material_basis_in heterozygous mutation in RRAS2 on chromosome 11p15.2."
    },
    "synonyms": [
        {
            "id": "DOID:0112170",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112170",
            "name": "NS12",
            "description": ""
        },
        {
            "id": "MIM:618624",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618624",
            "name": "Noonan syndrome 12",
            "description": "Noonan syndrome 12"
        }
    ]
}