{
  "id": 11285,
  "label": "taurodontism",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010098",
  "properties": {
    "xrefs": [
      "HP:0000679",
      "MEDGEN:75596",
      "MESH:C536946",
      "OMIM:272700",
      "Orphanet:3289",
      "SCTID:51744007",
      "UMLS:C0266039",
      "icd11.foundation:356382747"
    ],
    "synonyms": [
      "taurodontism",
      "taurodontism (disease)",
      "Bull teeth",
      "large pulp chambers in the molars"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0006858",
        "name": "mouth disorder"
      }
    ],
    "definition": "Taurodontism is a dental anomaly characterized by an elongated pulp chamber, displaced toward the apical floor of the tooth with no constriction at the level of the cemento-enamel junction, and short roots. It most frequently affects permanent molar teeth. Taurodontism increases the risk of pulp exposure. It can be isolated or associated with certain syndromes such as Down syndrome, amelogenesis imperfecta, and Klinefelter syndrome."
  },
  "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": 8422,
      "label": "tooth disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6893,
        8301
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1091",
          "EFO:1001216",
          "MEDGEN:11852",
          "MESH:D014076",
          "NCIT:C35077",
          "SCTID:234947003",
          "UMLS:C0040435"
        ],
        "synonyms": [
          "calcareous tooth disease",
          "calcareous tooth disease or disorder",
          "dental disorder",
          "disease of calcareous tooth",
          "disease or disorder of calcareous tooth",
          "disorder of calcareous tooth",
          "tooth disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ],
        "definition": "A disease involving the calcareous tooth."
      },
      "child_count": 22,
      "reference_id": "MONDO:0006999"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 8422,
      "label": "tooth disorder"
    }
  ]
}