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