{
  "id": 15768,
  "label": "Wilms tumor 6",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014779",
  "properties": {
    "xrefs": [
      "GARD:0016162",
      "MEDGEN:855962",
      "OMIM:616806",
      "UMLS:C3891301"
    ],
    "synonyms": [
      "WT6",
      "Wilms tumor 6",
      "Wilms tumor 6; WT6",
      "Wilms tumor type 6",
      "Wilms tumour 6; WT6",
      "Wilms tumour type 6",
      "Wilms tumor 6, susceptibility to",
      "Wilms tumour 6, susceptibility to"
    ],
    "definition": "Any Wilms tumor in which the cause of the disease is a mutation in the REST gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5261,
      "label": "hereditary Wilms tumor",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        7641
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5183",
          "GARD:0023447",
          "MEDGEN:146190",
          "NCIT:C8496",
          "OMIMPS:194070",
          "UMLS:C0677779"
        ],
        "synonyms": [
          "familial Wilms tumor",
          "familial Wilms tumour",
          "familial Wilms' tumor",
          "familial Wilms' tumour",
          "hereditary Wilms tumor",
          "hereditary kidney adenosarcoma",
          "hereditary nephroblastoma",
          "hereditary renal adenosarcoma",
          "WT1"
        ],
        "definition": "Familial embryonal neoplasm derived from nephrogenic blastemal cells. Several lines of differentiation, including blastemal, stromal and epithelial, are usually expressed. Comprises approximately 1% of Wilms tumors. (AFIP fascicle version 2.0)"
      },
      "child_count": 14,
      "reference_id": "MONDO:0003321"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5261,
      "label": "hereditary Wilms tumor"
    }
  ]
}