{
  "id": 13280,
  "label": "spondyloepiphyseal dysplasia tarda, autosomal recessive, Leroy-Spranger type",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012219",
  "properties": {
    "xrefs": [
      "DOID:0112291",
      "GARD:0024854",
      "MEDGEN:373126",
      "MESH:C563772",
      "OMIM:609223",
      "UMLS:C1836584"
    ],
    "synonyms": [
      "spondyloepiphyseal dysplasia tarda, autosomal recessive, Leroy-Spranger type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19453,
      "label": "spondyloepiphyseal dysplasia tarda",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17206
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112284",
          "GARD:0025144",
          "ICD9:756.9",
          "NORD:1732",
          "Orphanet:93284",
          "SCTID:51952004"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Spondyloepiphyseal dysplasia tarda (SEDT) is characterized by disproportionate short stature in adolescence or adulthood, associated with a short trunk and arms and barrel-shaped chest."
      },
      "child_count": 6,
      "reference_id": "MONDO:0019667"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19453,
      "label": "spondyloepiphyseal dysplasia tarda"
    }
  ]
}