{
  "id": 9224,
  "label": "hereditary leiomyomatosis and renal cell cancer",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007888",
  "properties": {
    "xrefs": [
      "GARD:0010096",
      "MEDGEN:353771",
      "MESH:C535516",
      "NCIT:C51302",
      "NORD:1231",
      "OMIM:150800",
      "Orphanet:523",
      "UMLS:C1708350",
      "icd11.foundation:754002573"
    ],
    "synonyms": [
      "HLRCC",
      "Hereditary Leiomyomatosis and Renal Cell Carcinoma",
      "MCUL",
      "Reed syndrome",
      "familial leiomyomatosis",
      "familial leiomyomatosis and renal cell cancer",
      "familial leiomyomatosis cutis et uteri",
      "familial leiomyomatosis with renal carcinoma",
      "familial multiple cutaneous leiomyomas",
      "hereditary leiomyomatosis",
      "hereditary leiomyomatosis and renal cell cancer",
      "hereditary leiomyomatosis and renal cell cancer syndrome",
      "hereditary leiomyomatosis and renal cell carcinoma",
      "hereditary leiomyomatosis with renal carcinoma",
      "hereditary multiple cutaneous leiomyomas",
      "leiomyomatosis and renal cell cancer",
      "multiple cutaneous and uterine leiomyomas",
      "LRCC",
      "Reed's syndrome",
      "leiomyoma, multiple cutaneous",
      "leiomyomatosis and renal cell cancer, hereditary",
      "leiomyomatosis familial",
      "multiple cutaneous and uterine leiomyomata",
      "multiple cutaneous and uterine leiomyomata 1, with or without renal cell carcinoma",
      "multiple cutaneous leiomyomata"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Hereditary leiomyomatosis and renal cell cancer (HLRCC) is a hereditary cancer syndrome characterized by a predisposition to cutaneous and uterine leiomyomas and, in some families, to renal cell cancer."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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": 16218,
      "label": "hereditary neoplastic syndrome"
    }
  ]
}