{
  "id": 24302,
  "label": "FANCM Fanconi-like genomic instability disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100578",
  "properties": {
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "FANCM Fanconi-like genomic instability disorder is autosomal recessive condition associated with an increased risk of cancer, infertility, and hypersensitivity to cytotoxic agents."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10460,
      "label": "Fanconi-like syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0090066",
          "MEDGEN:56237",
          "MESH:C536855",
          "OMIM:227850",
          "SCTID:236469003",
          "UMLS:C0151638"
        ],
        "synonyms": [
          "Fanconi-like syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A syndrome characterized by pancytopenia, immune deficiency and cutaneous malignancies."
      },
      "child_count": 2,
      "reference_id": "MONDO:0009217"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10460,
      "label": "Fanconi-like syndrome"
    }
  ]
}