{
    "disease_id": "DOID:0060578",
    "recommended_name": {
        "id": "DOID:0060578",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060578",
        "name": "Noonan syndrome 1",
        "description": "A Noonan syndrome that has_material_basis_in the PTPN11 gene on chromosome 12q24."
    },
    "synonyms": [
        {
            "id": "DOID:0060578",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060578",
            "name": "NS1",
            "description": ""
        },
        {
            "id": "MONDO:0008104",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008104",
            "name": "Noonan syndrome 1",
            "description": "Noonan syndrome caused by mutations in the PTPN11 gene."
        },
        {
            "id": "MONDO:0008104",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008104",
            "name": "NS1",
            "description": ""
        },
        {
            "id": "MONDO:0008104",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008104",
            "name": "Noonan syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0008104",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008104",
            "name": "Noonan syndrome type 1",
            "description": ""
        },
        {
            "id": "MIM:163950",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/163950",
            "name": "Noonan syndrome 1",
            "description": "Noonan syndrome 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060578"
    ],
    "unlinked_id_list": []
}