{
  "id": 10480,
  "label": "focal epithelial hyperplasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009237",
  "properties": {
    "xrefs": [
      "DOID:5362",
      "EFO:0007275",
      "ICD9:528.79",
      "MEDGEN:60066",
      "MESH:D017573",
      "NCIT:C97083",
      "OMIM:229045",
      "SCTID:6121001",
      "UMLS:C0206067"
    ],
    "synonyms": [
      "heck disease",
      "FEH, oral",
      "focal epithelial hyperplasia, oral"
    ],
    "definition": "Hyperplasia characterized by the presence of a focal proliferation of epithelial cells."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 6775,
      "label": "hyperplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23519
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0000536",
          "MEDGEN:43784",
          "MESH:D006965",
          "NCIT:C3113",
          "UMLS:C0020507"
        ],
        "synonyms": [
          "hyperplasia",
          "hyperplastic"
        ],
        "definition": "An abnormal increase in the number of cells in an organ or a tissue with consequent enlargement."
      },
      "child_count": 14,
      "reference_id": "MONDO:0005043"
    },
    {
      "id": 6834,
      "label": "viral infectious disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7200
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:934",
          "EFO:0000763",
          "ICD9:060-066",
          "ICD9:066.9",
          "ICD9:078.89",
          "ICD9:079.99",
          "MESH:D014777",
          "NCIT:C3439",
          "SCTID:34014006"
        ],
        "synonyms": [
          "Viruses caused disease or disorder",
          "Viruses disease or disorder",
          "Viruses infection",
          "Viruses infectious disease",
          "infection, viral",
          "viral disease",
          "viral disorder",
          "viral infection",
          "infections, Viruses"
        ],
        "definition": "Any disease caused by a virus."
      },
      "child_count": 42,
      "reference_id": "MONDO:0005108"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 6775,
      "label": "hyperplasia"
    },
    {
      "id": 6834,
      "label": "viral infectious disease"
    }
  ]
}