{
  "id": 9342,
  "label": "trismus-pseudocamptodactyly syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008016",
  "properties": {
    "xrefs": [
      "DOID:0111603",
      "GARD:0002621",
      "ICD9:759.89",
      "MEDGEN:78540",
      "MESH:C535857",
      "NORD:1795",
      "OMIM:158300",
      "Orphanet:3377",
      "SCTID:8757006",
      "UMLS:C0265226"
    ],
    "synonyms": [
      "Dutch-Kentucky syndrome",
      "Hecht syndrome",
      "Hecht-Beals syndrome",
      "distal arthrogryposis type 7",
      "trismus-pseudocamptodactyly syndrome",
      "DA7",
      "arthrogryposis distal type 7",
      "arthrogryposis, distal, type 7",
      "mouth, inability to open completely, and short finger-flexor tendons"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19660,
      "label": "distal arthrogryposis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        5798,
        16118
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050646",
          "GARD:0000786",
          "MEDGEN:120512",
          "OMIMPS:108120",
          "Orphanet:97120",
          "SCTID:24269006",
          "UMLS:C0265213",
          "icd11.foundation:1265239690"
        ],
        "synonyms": [
          "arthrogryposis multiplex congenita distal"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A muscle tissue disease characterized by congenital joint contractures of hand and feet."
      },
      "child_count": 69,
      "reference_id": "MONDO:0019942"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19660,
      "label": "distal arthrogryposis"
    }
  ]
}