{
  "id": 8588,
  "label": "axial osteomalacia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007181",
  "properties": {
    "xrefs": [
      "DOID:0080039",
      "GARD:0008431",
      "MEDGEN:354730",
      "MESH:C537791",
      "OMIM:109130",
      "UMLS:C1862372"
    ],
    "synonyms": [
      "axial osteomalacia",
      "atypical osteomalacia involving the axial skeleton"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 23099,
      "label": "familial osteosclerosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4938,
        5714
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "hereditary osteosclerosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "An instance of osteosclerosis that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 6,
      "reference_id": "MONDO:0042973"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23099,
      "label": "familial osteosclerosis"
    }
  ]
}