{
  "id": 18785,
  "label": "dentinogenesis imperfecta",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018849",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "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": [
    {
      "id": 8831,
      "label": "dentinogenesis imperfecta type 2",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        18785
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0012796",
          "MEDGEN:424922",
          "OMIM:125490",
          "Orphanet:166260",
          "UMLS:C2973527",
          "icd11.foundation:314718507"
        ],
        "synonyms": [
          "Capdepont teeth",
          "DGI-2",
          "DI-2",
          "dentinogenesis imperfecta type 1",
          "dentinogenesis imperfecta, Shields type 2",
          "dentinogenesis imperfecta, Shields type II",
          "DGI-II",
          "DGI1",
          "dentinogenesis imperfecta 1",
          "dentinogenesis imperfecta without osteogenesis imperfecta",
          "opalescent dentin",
          "opalescent teeth without osteogenesis imperfecta"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ],
        "definition": "Dentinogenesis imperfecta type 2 (DGI-2) is a rare, severe form of dentinogenesis imperfecta (DGI) and is characterized by weakness and discoloration of all teeth."
      },
      "child_count": 2,
      "reference_id": "MONDO:0007441"
    },
    {
      "id": 8832,
      "label": "dentinogenesis imperfecta type 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5714,
        18785
      ],
      "type_id": 0,
      "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)."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007442"
    }
  ],
  "roots": [
    {
      "id": 8422,
      "label": "tooth disorder"
    }
  ]
}