{
    "disease_id": "DOID:0080549",
    "recommended_name": {
        "id": "DOID:0080549",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080549",
        "name": "Noonan syndrome with multiple lentigines 2",
        "description": "A Noonan syndrome with multiple lentigines that has_material_basis_in heterozygous mutation in the RAF1 gene on chromosome 3p25."
    },
    "synonyms": [
        {
            "id": "DOID:0080549",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080549",
            "name": "LEOPARD syndrome 2",
            "description": ""
        },
        {
            "id": "MONDO:0012691",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012691",
            "name": "LEOPARD syndrome 2",
            "description": "Any Noonan syndrome with multiple lentigines in which the cause of the disease is a mutation in the RAF1 gene."
        },
        {
            "id": "MONDO:0012691",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012691",
            "name": "LEOPARD syndrome 2",
            "description": ""
        },
        {
            "id": "MONDO:0012691",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012691",
            "name": "Leopard syndrome type 2",
            "description": ""
        },
        {
            "id": "MONDO:0012691",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012691",
            "name": "leopard syndrome 2",
            "description": ""
        },
        {
            "id": "MONDO:0012691",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012691",
            "name": "LPRD2",
            "description": ""
        },
        {
            "id": "MIM:611554",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/611554",
            "name": "LEOPARD syndrome 2",
            "description": "LEOPARD syndrome 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080549"
    ],
    "unlinked_id_list": []
}