{
  "id": 17440,
  "label": "open iniencephaly",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017060",
  "properties": {
    "xrefs": [
      "GARD:0020949",
      "MEDGEN:608900",
      "Orphanet:268363",
      "SCTID:203928008",
      "UMLS:C0431285",
      "icd11.foundation:1778329323"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18889,
      "label": "iniencephaly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18236
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010506",
          "ICD10CM:Q00.2",
          "ICD9:740.2",
          "MEDGEN:57756",
          "MedDRA:10022034",
          "NCIT:C124549",
          "Orphanet:63259",
          "SCTID:2438005",
          "UMLS:C0152234",
          "icd11.foundation:1558931335"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Iniencephaly is a rare form of neural tube defect in which a malformation of the cervico-occipital junction is associated with a malformation of the central nervous system."
      },
      "child_count": 2,
      "reference_id": "MONDO:0018968"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18889,
      "label": "iniencephaly"
    }
  ]
}