{
  "id": 16050,
  "label": "multiple polyglandular tumor",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015079",
  "properties": {
    "xrefs": [
      "GARD:0019766",
      "ICD10WHO:D44.8",
      "MEDGEN:1863613",
      "Orphanet:100094",
      "UMLS:C5848154",
      "icd11.foundation:1316827435"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 16071,
      "label": "polyendocrinopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6875
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019800",
          "MEDGEN:1826133",
          "Orphanet:101956",
          "UMLS:C5681797"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 7,
      "reference_id": "MONDO:0015126"
    }
  ],
  "children": [
    {
      "id": 12529,
      "label": "Carney triad",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16050,
        20301
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010924",
          "MEDGEN:388099",
          "MESH:C565803",
          "NCIT:C94833",
          "OMIM:604287",
          "Orphanet:139411",
          "SCTID:733492003",
          "UMLS:C1858592",
          "icd11.foundation:1771169701"
        ],
        "synonyms": [
          "Carney triad",
          "gastric leiomyosarcoma, pulmonary chondroma, and extraadrenal paraganglioma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Carney's triad is a rare non-hereditary condition characterized by gastrointestinal stromal tumors (GIST, intramural mesenchymal tumors of the gastrointestinal tract with neuronal or neural crest cell origin), pulmonary chondromas and extraadrenal paragangliomas."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011424"
    },
    {
      "id": 12827,
      "label": "Carney-Stratakis syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16050,
        16218
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080533",
          "GARD:0010643",
          "MEDGEN:376098",
          "MESH:C564650",
          "NCIT:C94831",
          "OMIM:606864",
          "Orphanet:97286",
          "SCTID:722377004",
          "UMLS:C1847319"
        ],
        "synonyms": [
          "Carney dyad",
          "Carney-Stratakis dyad",
          "Carney-Stratakis syndrome",
          "gist-paraganglioma dyad",
          "paraganglioma and gastric stromal sarcoma",
          "Carney-Stratakis dyad of paraganglioma and gastric stromal sarcoma",
          "paraganglioma and gastrointestinal stromal tumor",
          "paraganglioma and gastrointestinal stromal tumour",
          "paraganglioma and gist"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Carney-Stratakis syndrome is a recently described familial syndrome characterized by gastrointestinal stromal tumors (GIST) and paragangliomas, often at multiple sites."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011740"
    },
    {
      "id": 17512,
      "label": "multiple endocrine neoplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16050,
        16218,
        20691
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3125",
          "GARD:0021044",
          "ICD10CM:E31.2",
          "ICD9:258.0",
          "ICDO:8360/1",
          "MEDGEN:45036",
          "MESH:D009377",
          "MedDRA:10061299",
          "NANDO:2100148",
          "NCIT:C6432",
          "OMIMPS:131100",
          "Orphanet:276161",
          "SCTID:46724008",
          "UMLS:C0027662"
        ],
        "synonyms": [
          "MEN",
          "men syndrome",
          "men syndromes",
          "multiple endocrine adenomatosis",
          "multiple endocrine neoplasia",
          "multiple endocrine neoplasia syndrome",
          "multiple endocrine neoplasia syndrome(s)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Multiple endocrine neoplasia (MEN) is a group of rare inherited cancer syndromes characterized by the development of two or more endocrine gland tumors, sometimes with tumor development in other tissues or organs."
      },
      "child_count": 9,
      "reference_id": "MONDO:0017169"
    }
  ],
  "roots": [
    {
      "id": 16071,
      "label": "polyendocrinopathy"
    }
  ]
}