{
    "disease_id": "DOID:0060587", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014691", 
            "name": "SOS2 Noonan syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014691", 
            "name": "Noonan syndrome 9; NS9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014691", 
            "name": "Noonan syndrome type 9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014691", 
            "name": "NS9"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014691", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014691", 
            "name": "Noonan syndrome caused by mutation in SOS2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060587", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060587", 
            "name": "NS9"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060587", 
        "description": "A Noonan syndrome that has_material_basis_in heterozygous mutation in the SOS2 gene on chromosome 14q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060587", 
        "name": "Noonan syndrome 9"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616559", 
            "id": "616559", 
            "database": "MIM"
        }
    ]
}