{
  "id": 9454,
  "label": "Thiemann disease, familial form",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008142",
  "properties": {
    "xrefs": [
      "GARD:0004131",
      "ICD9:716.84",
      "MEDGEN:82674",
      "MESH:C537144",
      "OMIM:165700",
      "Orphanet:3314",
      "SCTID:55166000",
      "UMLS:C0264081",
      "icd11.foundation:67016273"
    ],
    "synonyms": [
      "Osteochondrosis of phalangeal epiphyses",
      "aseptic necrosis of phalangeal epiphyses",
      "osteochondritis of phalangeal epiphyses",
      "THIEMANN disease",
      "Thiemann epiphyseal disease",
      "Thiemann's disease",
      "osteoarthropathy of fingers familial",
      "osteoarthropathy of fingers, familial"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "Thiemann disease is a very rare genetic necrotic bone disorder characterized clinically by painless swelling of the proximal interphalangeal joints associated with osteonecrosis of epiphyses followed by osteoarthritic changes, with onset before 25 years of age and often a benign course."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18460,
      "label": "osteochondrosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7060
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:8125",
          "GARD:0012704",
          "ICD10CM:M42",
          "ICD9:732.6",
          "MEDGEN:18216",
          "MESH:D055034",
          "NCIT:C34879",
          "Orphanet:399319",
          "SCTID:19579005",
          "UMLS:C0029429",
          "icd11.foundation:1446309782"
        ],
        "synonyms": [
          "osteochondrosis not specified as adult or juvenile, of unspecified site",
          "osteochondritis",
          "osteochondritis juvenilis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A condition that is characterized by defective bone growth that affects the growth centers of bone."
      },
      "child_count": 11,
      "reference_id": "MONDO:0018381"
    },
    {
      "id": 18462,
      "label": "osteonecrosis of genetic origin",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        7060
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021667",
          "MEDGEN:1842788",
          "Orphanet:399380",
          "UMLS:C5680035"
        ],
        "synonyms": [
          "bone necrosis of genetic origin",
          "genetic osteonecrosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "An instance of osteonecrosis that is caused by a modification of the individual's genome."
      },
      "child_count": 24,
      "reference_id": "MONDO:0018383"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18460,
      "label": "osteochondrosis"
    },
    {
      "id": 18462,
      "label": "osteonecrosis of genetic origin"
    }
  ]
}