{
  "id": 9642,
  "label": "contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008338",
  "properties": {
    "xrefs": [
      "DOID:0081321",
      "GARD:0013058",
      "MEDGEN:401232",
      "MESH:C566739",
      "OMIM:178110",
      "Orphanet:65743",
      "UMLS:C1867440"
    ],
    "synonyms": [
      "contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A",
      "distal arthrogryposis type 8",
      "multiple pterygium syndrome, autosomal dominant",
      "DA8",
      "arthrogryposis, distal, type 8",
      "pterygium syndrome, multiple, autosomal dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2903,
      "label": "autosomal dominant disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050736",
          "ICD9:758.5",
          "MEDGEN:539206",
          "SCTID:11164009",
          "UMLS:C0265385"
        ],
        "synonyms": [
          "autosomal dominant disease or disorder",
          "autosomal dominant hereditary disorder",
          "autosomal dominant inherited disorder",
          "disease or disorder, autosomal dominant",
          "disease, autosomal dominant"
        ],
        "definition": "Autosomal dominant form of disease."
      },
      "child_count": 192,
      "reference_id": "MONDO:0000426"
    },
    {
      "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"
    },
    {
      "id": 20245,
      "label": "contractures, pterygia, and variable skeletal fusions syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        17720
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025269",
          "OMIMPS:178110"
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0020937"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2903,
      "label": "autosomal dominant disease"
    },
    {
      "id": 19660,
      "label": "distal arthrogryposis"
    },
    {
      "id": 20245,
      "label": "contractures, pterygia, and variable skeletal fusions syndrome"
    }
  ]
}