{
  "id": 8826,
  "label": "dentin dysplasia type I",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007436",
  "properties": {
    "xrefs": [
      "GARD:0001807",
      "ICD9:520.5",
      "MEDGEN:97996",
      "MESH:C531665",
      "MESH:C538215",
      "NORD:1041",
      "OMIMPS:125400",
      "Orphanet:99789",
      "SCTID:109493006",
      "UMLS:C0399379"
    ],
    "synonyms": [
      "DD-I",
      "DTDP1",
      "dentin dysplasia type I",
      "dentin dysplasia, type i, with microdontia and misshapen teeth",
      "radicular dentin dysplasia",
      "dentin dysplasia, Shields type 1",
      "dentin dysplasia, type 1",
      "dentin dysplasia, type I",
      "dentin dysplasia, type I, with extreme microdontia and misshapen teeth",
      "rootless teeth"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0006858",
        "name": "mouth disorder"
      }
    ],
    "definition": "Dentin dysplasia type I (DD-I) is a rare form of dentin dysplasia (DD) characterized by sharp conical short roots or rootless teeth."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "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": [
    {
      "id": 18040,
      "label": "atypical dentin dysplasia due to SMOC2 deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8826
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017433",
          "MEDGEN:1673452",
          "OMIM:125400",
          "Orphanet:314721",
          "UMLS:C5190802"
        ],
        "synonyms": [
          "dentin dysplasia type 1 with microdontia and shape anomalies",
          "dentin dysplasia, type IA"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0017819"
    },
    {
      "id": 24760,
      "label": "dentin dysplasia, type IB",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8826
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "OMIM:621440"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0700387"
    }
  ],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 16407,
      "label": "dentin dysplasia"
    }
  ]
}