{
    "disease_id": "DOID:0060584",
    "recommended_name": {
        "id": "DOID:0060584",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060584",
        "name": "Noonan syndrome 6",
        "description": "A Noonan syndrome that has_material_basis_in heterozygous mutation in the NRAS gene on chromosome 1p13."
    },
    "synonyms": [
        {
            "id": "DOID:0060584",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060584",
            "name": "NS6",
            "description": ""
        },
        {
            "id": "MONDO:0013186",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013186",
            "name": "Noonan syndrome 6",
            "description": "Any Noonan syndrome in which the cause of the disease is a mutation in the NRAS gene."
        },
        {
            "id": "MONDO:0013186",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013186",
            "name": "NRAS Noonan syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013186",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013186",
            "name": "NS6",
            "description": ""
        },
        {
            "id": "MONDO:0013186",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013186",
            "name": "Noonan syndrome 6",
            "description": ""
        },
        {
            "id": "MONDO:0013186",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013186",
            "name": "Noonan syndrome caused by mutation in NRAS",
            "description": ""
        },
        {
            "id": "MONDO:0013186",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013186",
            "name": "Noonan syndrome type 6",
            "description": ""
        },
        {
            "id": "MONDO:0013186",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013186",
            "name": "NRAS gene related Noonan syndrome",
            "description": ""
        },
        {
            "id": "MIM:613224",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613224",
            "name": "Noonan syndrome 6",
            "description": "Noonan syndrome 6"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060584"
    ],
    "unlinked_id_list": []
}