{
    "disease_id": "DOID:0061217",
    "recommended_name": {
        "id": "DOID:0061217",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061217",
        "name": "pheochromocytoma/paraganglioma syndrome 2",
        "description": "A paraganglioma characterized by the development of neuroendocrine tumors, usually in adulthood that has material_basis_in heterozygous mutation in the SDHAF2 gene."
    },
    "synonyms": [
        {
            "id": "MONDO:0011121",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011121",
            "name": "pheochromocytoma/paraganglioma syndrome 2",
            "description": "An autosomal dominant tumor predisposition disorder caused by pathogenic variants in the SDHAF2 gene, characterized by an increased risk of paraganglioma, particularly head and neck paragangliomas."
        },
        {
            "id": "MONDO:0011121",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011121",
            "name": "SDHAF2 paraganglioma",
            "description": ""
        },
        {
            "id": "MONDO:0011121",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011121",
            "name": "SDHAF2-related tumor predisposition",
            "description": ""
        },
        {
            "id": "MONDO:0011121",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011121",
            "name": "paraganglioma caused by mutation in SDHAF2",
            "description": ""
        },
        {
            "id": "MONDO:0011121",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011121",
            "name": "paragangliomas 2",
            "description": ""
        },
        {
            "id": "MONDO:0011121",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011121",
            "name": "paragangliomas type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011121",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011121",
            "name": "pheochromocytoma/paraganglioma syndrome 2",
            "description": ""
        },
        {
            "id": "MONDO:0011121",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011121",
            "name": "PGL2",
            "description": ""
        },
        {
            "id": "MONDO:0011121",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011121",
            "name": "SDHAF2-related hereditary paraganglioma-pheochromocytoma syndrome (paragangliomas 2)",
            "description": ""
        },
        {
            "id": "MIM:601650",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/601650",
            "name": "Pheochromocytoma/paraganglioma syndrome 2",
            "description": "Pheochromocytoma/paraganglioma syndrome 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061217"
    ],
    "unlinked_id_list": []
}