{
  "id": 12827,
  "label": "Carney-Stratakis syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011740",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16050,
      "label": "multiple polyglandular tumor",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16071
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019766",
          "ICD10WHO:D44.8",
          "MEDGEN:1863613",
          "Orphanet:100094",
          "UMLS:C5848154",
          "icd11.foundation:1316827435"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0015079"
    },
    {
      "id": 16218,
      "label": "hereditary neoplastic syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        20011,
        20301
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019921",
          "MEDGEN:14326",
          "MESH:D009386",
          "NCIT:C3266",
          "Orphanet:140162",
          "SCTID:699346009",
          "UMLS:C0027672"
        ],
        "synonyms": [
          "cancer syndrome, hereditary",
          "cancer syndromes, hereditary",
          "familial neoplastic syndrome",
          "familial tumor syndrome",
          "familial tumour syndrome",
          "hereditary cancer syndrome",
          "hereditary cancer syndromes",
          "hereditary neoplastic syndrome",
          "hereditary neoplastic syndromes",
          "hereditary tumor syndrome",
          "hereditary tumour syndrome",
          "inherited cancer syndrome",
          "inherited cancer-predisposing syndrome",
          "neoplastic syndrome, hereditary",
          "syndrome, hereditary cancer",
          "syndrome, hereditary neoplastic",
          "syndromes, hereditary cancer",
          "syndromes, hereditary neoplastic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "The inherited predisposition toward getting a tumor."
      },
      "child_count": 351,
      "reference_id": "MONDO:0015356"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16050,
      "label": "multiple polyglandular tumor"
    },
    {
      "id": 16218,
      "label": "hereditary neoplastic syndrome"
    }
  ]
}