{
  "id": 9019,
  "label": "familial ossifying fibroma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007660",
  "properties": {
    "xrefs": [
      "GARD:0017713",
      "MEDGEN:501159",
      "MESH:C563017",
      "OMIM:137575",
      "Orphanet:435329",
      "UMLS:C3495361"
    ],
    "synonyms": [
      "hereditary ossifying fibroma (disease)",
      "multiple ossifying fibroma",
      "Cementomas, familial multiple",
      "GIGANTIFORM cementoma, familial",
      "Jaffe-Campanacci syndrome",
      "cemental dysplasia, periapical",
      "intracortical fibrous dysplasia"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      }
    ],
    "definition": "An instance of ossifying fibroma (disease) that is caused by an inherited modification of the individual's genome."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4254,
      "label": "ossifying fibroma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3036
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:180",
          "GARD:0012792",
          "HP:0030426",
          "ICDO:9262/0",
          "ICDO:9274/0",
          "MEDGEN:104906",
          "MESH:D018214",
          "NCIT:C173820",
          "NCIT:C8422",
          "NORD:111729",
          "UMLS:C0206640"
        ],
        "synonyms": [
          "Cementifying fibroma",
          "cemento-ossifying fibroma",
          "fibroma, ossifying, benign",
          "ossifying fibroma",
          "ossifying fibroma (disease)",
          "Juvenile Ossifying Fibroma",
          "juvenile ossifying fibroma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A well circumscribed lesion of the bone, most frequently arising from the posterior mandible. It is characterized by the presence of fibrous tissue and a mineralized component which may be woven bone, lamellar bone, or cementum-like material. Complete removal is recommended, since it continues to enlarge if left untreated."
      },
      "child_count": 1,
      "reference_id": "MONDO:0002119"
    },
    {
      "id": 21247,
      "label": "hereditary disorder of connective tissue",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        5762
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:473110",
          "NCIT:C97075",
          "SCTID:363045008",
          "UMLS:C0410787"
        ],
        "synonyms": [
          "Mendelian connective tissue disorder",
          "connective tissue hereditary disorder",
          "hereditary connective tissue disorder",
          "Hereditary Connective Tissue Disorder",
          "Inherited disorder of connective tissue",
          "inherited disorder of connective tissue"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "An inherited genetic disorder that affects the connective tissues. Representative examples include Ehlers-Danlos syndrome and Marfan syndrome."
      },
      "child_count": 176,
      "reference_id": "MONDO:0023603"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4254,
      "label": "ossifying fibroma"
    },
    {
      "id": 21247,
      "label": "hereditary disorder of connective tissue"
    }
  ]
}