{
  "id": 9955,
  "label": "Wilms tumor 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008680",
  "properties": {
    "xrefs": [
      "GARD:0008559",
      "MEDGEN:854562",
      "MESH:C536853",
      "OMIM:194071",
      "UMLS:C3887743"
    ],
    "synonyms": [
      "Wilms tumor 2",
      "Wilms tumor 2, autosomal dominant, somatic mutation",
      "Wilms tumor type 2",
      "Wilms tumour 2, autosomal dominant, somatic mutation",
      "Wilms tumour type 2",
      "FWT2",
      "WT2",
      "familial Wilms tumor 2",
      "familial Wilms tumour 2"
    ]
  },
  "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"
    }
  ]
}