{
    "disease_id": "DOID:0112170", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0112170", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112170", 
            "name": "NS12"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112170", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112170", 
        "name": "Noonan syndrome 12"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618624", 
            "id": "618624", 
            "database": "MIM"
        }
    ]
}