{
  "id": 20080,
  "label": "Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020667",
  "properties": {
    "xrefs": [
      "DOID:0081290",
      "GARD:0022389",
      "MEDGEN:422448",
      "OMIM:207410",
      "Orphanet:596008",
      "UMLS:C2936791"
    ],
    "synonyms": [
      "Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis",
      "ABS2",
      "multisynostotic osteodysgenesis with long bone fractures",
      "osteodysgenesis, multisynostotic, with fractures",
      "trapezoidocephaly-synostosis Syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10074,
      "label": "Antley-Bixler syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        12769,
        16088,
        16201
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050462",
          "DOID:0081289",
          "GARD:0005826",
          "MEDGEN:1714404",
          "NANDO:1200669",
          "NANDO:2200975",
          "NORD:792",
          "Orphanet:83",
          "SCTID:62964007",
          "UMLS:C5234850",
          "icd11.foundation:2027710139"
        ],
        "synonyms": [
          "Antley Bixler syndrome",
          "multisynostotic osteodysgenesis with long bone fractures",
          "osteodysgenesis, multisynostotic with fractures",
          "osteodysgenesis, multisynostotic, with fractures",
          "trapezoidocephaly synostosis syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Antley-Bixler syndrome is a very rare disorder characterized by craniosynostosis with midface hypoplasia, radiohumeral synostosis, femoral bowing and joint contractures."
      },
      "child_count": 6,
      "reference_id": "MONDO:0008803"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10074,
      "label": "Antley-Bixler syndrome"
    }
  ]
}