{
  "id": 8827,
  "label": "dentin dysplasia type II",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007437",
  "properties": {
    "xrefs": [
      "GARD:0001806",
      "ICD9:520.5",
      "MEDGEN:96026",
      "OMIM:125420",
      "Orphanet:99791",
      "SCTID:109494000",
      "UMLS:C0399380"
    ],
    "synonyms": [
      "DD-II",
      "DTDP2",
      "Dtdp2",
      "anomalous dysplasia of dentin",
      "coronal dentin dysplasia",
      "dentin dyspalsia, Shields type 2",
      "dentin dysplasia, Shields type 2",
      "dentin dysplasia, coronal",
      "dentin dysplasia, type 2",
      "dentin dysplasia, type II",
      "pulp stones",
      "pulpal dysplasia"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0006858",
        "name": "mouth disorder"
      }
    ],
    "definition": "Dentin dysplasia type II (DD-II) is a rare mild form of dentin dysplasia (DD) characterized by normal tooth roots but abnormal primary dentition."
  },
  "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": 16407,
      "label": "dentin dysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4339
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:701",
          "GARD:0016575",
          "ICD9:520.5",
          "MEDGEN:8310",
          "MESH:D003805",
          "Orphanet:1653",
          "SCTID:109492001",
          "UMLS:C0011430",
          "icd11.foundation:1262020657"
        ],
        "synonyms": [
          "DD"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ],
        "definition": "Dentin dysplasia (DD) is a rare disorder belonging to the group of hereditary dentin defects and is characterized by abnormal dentin structure and root development resulting in abnormal tooth development. It encompasses two subtypes: DD type I and DD type II."
      },
      "child_count": 2,
      "reference_id": "MONDO:0015613"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 16407,
      "label": "dentin dysplasia"
    }
  ]
}