{
  "id": 8832,
  "label": "dentinogenesis imperfecta type 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007442",
  "properties": {
    "xrefs": [
      "GARD:0010144",
      "ICD9:520.5",
      "MEDGEN:97995",
      "MESH:C538216",
      "NORD:1043",
      "OMIM:125500",
      "Orphanet:166265",
      "SCTID:234970006",
      "UMLS:C0399378",
      "icd11.foundation:518257495"
    ],
    "synonyms": [
      "DGI-III",
      "Dentinogenesis Imperfecta Type III",
      "brandywine type dentinogenesis imperfecta",
      "dentinogenesis imperfecta Shields type 3",
      "dentinogenesis imperfecta type III",
      "dentinogenesis imperfecta, Shields type 3",
      "dentinogenesis imperfecta, Shields type III"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0006858",
        "name": "mouth disorder"
      }
    ],
    "definition": "Dentinogenesis imperfecta type 3 (DGI-3) is a rare, severe form of dentinogenesis imperfecta (DGI) characterized by opalescent primary and permanent teeth, marked attrition, large pulp chambers, multiple pulp exposure and shell teeth radiographically (i.e. teeth which appear hollow due to dentin hypotrophy)."
  },
  "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": 18785,
      "label": "dentinogenesis imperfecta",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8422
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4154",
          "GARD:0006258",
          "HP:0000703",
          "ICD9:520.5",
          "MEDGEN:8313",
          "MESH:D003811",
          "MedDRA:10054013",
          "NCIT:C84667",
          "Orphanet:49042",
          "SCTID:196286005",
          "UMLS:C0011436",
          "icd11.foundation:2090257992"
        ],
        "synonyms": [
          "DGI",
          "DGI without OI",
          "DI",
          "dentinogenesis imperfecta",
          "dentinogenesis imperfecta (disease)",
          "dentinogenesis imperfecta without osteogenesis imperfecta",
          "non-syndromic DGI",
          "non-syndromic dentinogenesis imperfecta",
          "opalescent teeth without OI",
          "opalescent teeth without osteogenesis imperfecta"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ],
        "definition": "Dentinogenesis imperfecta (DGI) is a hereditary dentin defect characterized by abnormal dentin structure resulting in abnormal tooth development."
      },
      "child_count": 2,
      "reference_id": "MONDO:0018849"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 18785,
      "label": "dentinogenesis imperfecta"
    }
  ]
}