{
    "disease_id": "DOID:0061218",
    "recommended_name": {
        "id": "DOID:0061218",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061218",
        "name": "pheochromocytoma/paraganglioma syndrome 3",
        "description": "A paraganglioma characterized by the development of neuroendocrine tumors, usually in adulthood that has material_basis_in heterozygous mutation in the SDHC gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0011544",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011544",
            "name": "pheochromocytoma/paraganglioma syndrome 3",
            "description": "An autosomal dominant tumor predisposition disorder caused by pathogenic variants in the SDHC gene, characterized by an increased risk of paraganglioma and pheochromocytoma, as well as an increased risk of renal cell carcinoma and gastrointestinal stromal tumors (GIST)."
        },
        {
            "id": "MONDO:0011544",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011544",
            "name": "SDHC paraganglioma",
            "description": ""
        },
        {
            "id": "MONDO:0011544",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011544",
            "name": "SDHC-related tumor predisposition",
            "description": ""
        },
        {
            "id": "MONDO:0011544",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011544",
            "name": "paraganglioma caused by mutation in SDHC",
            "description": ""
        },
        {
            "id": "MONDO:0011544",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011544",
            "name": "paragangliomas 3",
            "description": ""
        },
        {
            "id": "MONDO:0011544",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011544",
            "name": "paragangliomas type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011544",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011544",
            "name": "pheochromocytoma/paraganglioma syndrome 3",
            "description": ""
        },
        {
            "id": "MONDO:0011544",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011544",
            "name": "PGL3",
            "description": ""
        },
        {
            "id": "MONDO:0011544",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011544",
            "name": "SDHC-related hereditary paraganglioma-pheochromocytoma syndrome (paragangliomas 3)",
            "description": ""
        },
        {
            "id": "MIM:605373",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/605373",
            "name": "Pheochromocytoma/paraganglioma syndrome 3",
            "description": "Pheochromocytoma/paraganglioma syndrome 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061218"
    ],
    "unlinked_id_list": []
}