{
  "id": 12667,
  "label": "deafness, autosomal dominant 39, with dentinogenesis imperfecta 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011571",
  "properties": {
    "xrefs": [
      "GARD:0015383",
      "MEDGEN:340145",
      "MESH:C565316",
      "OMIM:605594",
      "UMLS:C1854146"
    ],
    "synonyms": [
      "deafness, autosomal dominant 39, with dentinogenesis imperfecta 1",
      "deafness, autosomal dominant 39, with dentinogenesis imperfecta type 1",
      "deafness, autosomal dominant 39, with dentinogenesis",
      "Dfna39/Dgi1 syndrome",
      "Dfna39/dentinogenesis imperfecta 1 syndrome",
      "Dgi1/Dfna39 syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0006858",
        "name": "mouth disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8831,
      "label": "dentinogenesis imperfecta type 2"
    }
  ]
}