{
    "disease_id": "DOID:0061216",
    "recommended_name": {
        "id": "DOID:0061216",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061216",
        "name": "pheochromocytoma/paraganglioma syndrome 1",
        "description": "A paraganglioma characterized by the development of neuroendocrine tumors, usually in adulthood that has material_basis_in heterozygous mutation in the SDHD gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0008192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008192",
            "name": "pheochromocytoma/paraganglioma syndrome 1",
            "description": "An autosomal dominant tumor predisposition disorder caused by pathogenic variants in the SDHD 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:0008192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008192",
            "name": "SDHD paraganglioma",
            "description": ""
        },
        {
            "id": "MONDO:0008192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008192",
            "name": "SDHD-related tumor predisposition",
            "description": ""
        },
        {
            "id": "MONDO:0008192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008192",
            "name": "paraganglioma caused by mutation in SDHD",
            "description": ""
        },
        {
            "id": "MONDO:0008192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008192",
            "name": "paragangliomas 1",
            "description": ""
        },
        {
            "id": "MONDO:0008192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008192",
            "name": "paragangliomas 1, with or without deafness",
            "description": ""
        },
        {
            "id": "MONDO:0008192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008192",
            "name": "paragangliomas type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008192",
            "name": "pheochromocytoma/paraganglioma syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0008192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008192",
            "name": "PGL1",
            "description": ""
        },
        {
            "id": "MONDO:0008192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008192",
            "name": "carotid body tumours",
            "description": ""
        },
        {
            "id": "MONDO:0008192",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008192",
            "name": "glomus jugulare tumours",
            "description": ""
        },
        {
            "id": "MIM:168000",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/168000",
            "name": "Pheochromocytoma/paraganglioma syndrome 1",
            "description": "Pheochromocytoma/paraganglioma syndrome 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061216"
    ],
    "unlinked_id_list": []
}