{
  "id": 25991,
  "label": "myelic limited dorsal malformation",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0970964",
  "properties": {
    "xrefs": [
      "GARD:0027096",
      "MEDGEN:1853142",
      "Orphanet:645378",
      "UMLS:C5816714"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A rare intermediate form of open dysraphism between myelomeningocele and saccular limited dorsal myeloschisis without fulfilling the characteristics of one of these two diagnosis, characterized by stretched neurulated spinal cord attached at the dome of a sac. Partial cerebral signs of open dysraphism can be observed and the meningocele is usually poorly epithelialized."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 25974,
      "label": "saccular spinal dysraphism with a stalk to the dome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17449,
        25942
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027084",
          "MEDGEN:1853133",
          "Orphanet:645319",
          "UMLS:C5816721"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare spinal dysraphism characterized by a meningocele, containing a stalk, that is attached to the inner surface of the meningocele. The stalk can be posteriorly fibroneural (saccular limited dorsal myeloschisis) or the spinal cord itself (myelic limited dorsal malformation)."
      },
      "child_count": 6,
      "reference_id": "MONDO:0968988"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 25974,
      "label": "saccular spinal dysraphism with a stalk to the dome"
    }
  ]
}