{
    "disease_id": "DOID:0060586",
    "recommended_name": {
        "id": "DOID:0060586",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060586",
        "name": "Noonan syndrome 8",
        "description": "A Noonan syndrome that has_material_basis_in caused by heterozygous mutation in the RIT1 gene on chromosome 1q22."
    },
    "synonyms": [
        {
            "id": "DOID:0060586",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060586",
            "name": "NS8",
            "description": ""
        },
        {
            "id": "MONDO:0014143",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014143",
            "name": "Noonan syndrome 8",
            "description": "Any Noonan syndrome in which the cause of the disease is a mutation in the RIT1 gene."
        },
        {
            "id": "MONDO:0014143",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014143",
            "name": "NS8",
            "description": ""
        },
        {
            "id": "MONDO:0014143",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014143",
            "name": "Noonan syndrome 8",
            "description": ""
        },
        {
            "id": "MONDO:0014143",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014143",
            "name": "Noonan syndrome caused by mutation in RIT1",
            "description": ""
        },
        {
            "id": "MONDO:0014143",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014143",
            "name": "Noonan syndrome type 8",
            "description": ""
        },
        {
            "id": "MONDO:0014143",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014143",
            "name": "RIT1 Noonan syndrome",
            "description": ""
        },
        {
            "id": "MIM:615355",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615355",
            "name": "Noonan syndrome 8",
            "description": "Noonan syndrome 8"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060586"
    ],
    "unlinked_id_list": []
}