{
  "id": 25948,
  "label": "hemi-myeloschisis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0958351",
  "properties": {
    "xrefs": [
      "GARD:0027025",
      "MEDGEN:1853138",
      "Orphanet:645393",
      "UMLS:C5816709"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A very rare form of composite dysraphism characterized by the presence of a split cord malformation and a myeloschisis on one of the two hemicords. Hemicords can be in a single dural sac or in two separated dural sacs. Other spinal cord malformations can be associated. Due to the comparable prognosis it is considered as a subtype of myeloschisis."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 25810,
      "label": "myeloschisis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17442
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026919",
          "MEDGEN:539965",
          "Orphanet:645398",
          "UMLS:C0266507",
          "icd11.foundation:1547705800"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare form of spina bifida/open neural tube defect (NTD) chacterized by absence of a cystic component, dysplastic meninges and neural placode exposed through a defect in the posterior vertebral arches (spina bifida) that are contiguous with surrounding skin. The placode is at or below the skin plane and is typically associated with a Chiari II malformation. It is usually isolated or rarely associated with split cord malformation."
      },
      "child_count": 2,
      "reference_id": "MONDO:0958076"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 25810,
      "label": "myeloschisis"
    }
  ]
}