{
  "id": 26420,
  "label": "spondylocostal dysostosis 7, autosomal recessive",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0981023",
  "properties": {
    "xrefs": [
      "OMIM:621523"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2864,
      "label": "spondylocostal dysostosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3140,
        5714,
        18362
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050568",
          "GARD:0012174",
          "MEDGEN:82707",
          "MESH:C537565",
          "NCIT:C125598",
          "NORD:1308",
          "OMIMPS:277300",
          "UMLS:C0265343"
        ],
        "synonyms": [
          "Spondylocostal Dysplasia",
          "costovertebral dysplasia",
          "spondylocostal dysostosis",
          "spondylocostal dysplasia",
          "Jarcho-Levin syndrome",
          "SCD",
          "SCDO"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Spondylocostal dysplasia is a rare genetic disorder characterized by defects of the bones of the spine (vertebrae) and abnormalities of the ribs. Ribs can be fused or missing in chaotic patterns. These malformations are present at birth (congenital)."
      },
      "child_count": 12,
      "reference_id": "MONDO:0000359"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2864,
      "label": "spondylocostal dysostosis"
    }
  ]
}