{
  "id": 8847,
  "label": "digitotalar dysmorphism; ulnar drift, hereditary",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007458",
  "properties": {
    "xrefs": [
      "GARD:0015059",
      "MEDGEN:342156",
      "OMIM:126050",
      "UMLS:C1852085"
    ],
    "synonyms": [
      "digitotalar dysmorphism",
      "ulnar drift, hereditary"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16130,
      "label": "digitotalar dysmorphism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16089,
        19660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111596",
          "GARD:0000787",
          "MESH:C565097",
          "Orphanet:1146",
          "icd11.foundation:1679749810"
        ],
        "synonyms": [
          "DA1",
          "arthrogryposis multiplex congenita distal type 1",
          "digitotalar dysmorphism",
          "distal arthrogryposis type 1",
          "distal arthrogryposis type 1A (sub-type)",
          "distal arthrogryposis type 1B (sub-type)",
          "AMCD1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Digitotalar dysmorphism, also known as distal arthrogryposis type 1 (DA1), is an autosomal dominant congenital anomaly characterized by contractures of the distal regions of the hands and feet with no facial involvement or any additional anomalies. It is the most common type of distal arthrogryposis."
      },
      "child_count": 6,
      "reference_id": "MONDO:0015240"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16130,
      "label": "digitotalar dysmorphism"
    }
  ]
}