{
  "id": 9344,
  "label": "Muir-Torre syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008018",
  "properties": {
    "xrefs": [
      "DOID:0050465",
      "GARD:0006821",
      "MEDGEN:231157",
      "MESH:D055653",
      "MedDRA:10063042",
      "NCIT:C84905",
      "OMIM:158320",
      "Orphanet:587",
      "SCTID:403824007",
      "UMLS:C1321489",
      "icd11.foundation:229304403"
    ],
    "synonyms": [
      "Muir-Torre syndrome",
      "multiple keratoacanthoma, Muir-Torre type",
      "MRTES",
      "MUIR-Torre syndrome",
      "cutaneous sebaceous neoplasms and keratoacanthomas multiple with gastrointestinal and other carcinomas",
      "cutaneous sebaceous neoplasms and keratoacanthomas, multiple, with gastrointestinal and Other carcinomas"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "Muir-Torre syndrome (MTS) is a form of hereditary nonpolyposis colon cancer (HNPCC) characterized by cutaneous sebaceous tumors, keratoacanthomas and at least one visceral malignancy, most frequently gastrointestinal carcinoma."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2903,
      "label": "autosomal dominant disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050736",
          "ICD9:758.5",
          "MEDGEN:539206",
          "SCTID:11164009",
          "UMLS:C0265385"
        ],
        "synonyms": [
          "autosomal dominant disease or disorder",
          "autosomal dominant hereditary disorder",
          "autosomal dominant inherited disorder",
          "disease or disorder, autosomal dominant",
          "disease, autosomal dominant"
        ],
        "definition": "Autosomal dominant form of disease."
      },
      "child_count": 192,
      "reference_id": "MONDO:0000426"
    },
    {
      "id": 18627,
      "label": "hereditary nonpolyposis colon cancer",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16218,
        21140
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025132",
          "MEDGEN:232602",
          "NCIT:C120083",
          "OMIMPS:120435",
          "Orphanet:443909",
          "SCTID:315058005",
          "UMLS:C1333990",
          "icd11.foundation:8113015"
        ],
        "synonyms": [
          "HNPCC",
          "Hereditary nonpolyposis colorectal cancer (HNPCC)",
          "colorectal cancer, hereditary nonpolyposis",
          "familial nonpolyposis colon cancer",
          "familial nonpolyposis colorectal cancer",
          "hereditary nonpolyposis colon cancer",
          "hereditary nonpolyposis colorectal cancer"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A cancer-predisposing condition characterized by the development of colorectal cancer not associated with colorectal polyposis, endometrial cancer, and various other cancers (such as malignant epithelial tumor of ovary, gastric, biliary tract, small bowel, and urinary tract cancer) that are frequently diagnosed at an early age."
      },
      "child_count": 10,
      "reference_id": "MONDO:0018630"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2903,
      "label": "autosomal dominant disease"
    },
    {
      "id": 18627,
      "label": "hereditary nonpolyposis colon cancer"
    }
  ]
}