{
  "id": 13544,
  "label": "spondyloepimetaphyseal dysplasia, Genevieve type",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012495",
  "properties": {
    "xrefs": [
      "DOID:0080576",
      "GARD:0010057",
      "MEDGEN:355314",
      "MESH:C535785",
      "OMIM:610442",
      "Orphanet:168454",
      "UMLS:C1864872",
      "icd11.foundation:1383217537"
    ],
    "synonyms": [
      "SEMD, Geneviève type",
      "SEMDG",
      "spondyloepimetaphyseal dysplasia, Camera-Genevieve type",
      "spondyloepimetaphyseal dysplasia, Genevieve type",
      "Nans deficiency",
      "SEMD Genevieve type",
      "SEMD, Genevieve type",
      "spondyloepimetaphyseal dysplasia Genevieve type",
      "spondyloepimetaphyseal dysplasia, Geneviève type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "A rare primary bone dysplasia characterized by severe developmental delay and skeletal dysplasia (including short stature, premature carpal ossification, platyspondyly, longitudinal metaphyseal striations, and small epiphyses), as well as moderate to severe intellectual disability and facial dysmorphism, including prominent forehead, mild synophrys, depressed nasal bridge, prominent bulbous nasal tip and full lips."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24235,
      "label": "spondyloepimetaphyseal dysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7171
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080027",
          "GARD:0026258",
          "MEDGEN:609408",
          "SCTID:254062008",
          "UMLS:C0432211"
        ],
        "synonyms": [
          "SEMD",
          "spondylo-epi-(meta)-physeal dysplasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "An osteochondrodysplasia that results in abnormalities of bone growth in the vertebral column, epiphysis, and metaphysis."
      },
      "child_count": 23,
      "reference_id": "MONDO:0100510"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24235,
      "label": "spondyloepimetaphyseal dysplasia"
    }
  ]
}