{
  "id": 11452,
  "label": "terminal osseous dysplasia-pigmentary defects syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010279",
  "properties": {
    "xrefs": [
      "DOID:0112149",
      "GARD:0016769",
      "MEDGEN:335344",
      "MESH:C564554",
      "OMIM:300244",
      "Orphanet:88630",
      "UMLS:C1846129"
    ],
    "synonyms": [
      "terminal osseous dysplasia, X-linked dominant",
      "Odpd",
      "Odpf syndrome",
      "TOD",
      "osseous dysplasia, digital, with Facial pigmentary defects and multiple frenula",
      "terminal osseous dysplasia",
      "terminal osseous dysplasia and pigmentary defects"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "A syndrome characterized by malformation of the hands and feet, pigmentary skin lesions on the face and scalp and digital fibromatosis."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19470,
      "label": "filamin-related bone disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18360
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019190",
          "MEDGEN:1842239",
          "Orphanet:93425",
          "UMLS:C5680280"
        ],
        "synonyms": [
          "bone filaminopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0019690"
    },
    {
      "id": 19473,
      "label": "acromelic dysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18360
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019194",
          "MEDGEN:1843369",
          "Orphanet:93436",
          "UMLS:C4736195",
          "icd11.foundation:177141175"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 18,
      "reference_id": "MONDO:0019695"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19470,
      "label": "filamin-related bone disorder"
    },
    {
      "id": 19473,
      "label": "acromelic dysplasia"
    }
  ]
}