{
  "id": 25989,
  "label": "terminal myelocystocele",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0970962",
  "properties": {
    "xrefs": [
      "GARD:0027094",
      "MEDGEN:1853147",
      "Orphanet:645337",
      "UMLS:C5816718"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A rare closed spinal dysraphism characterized by a myelocystocele at the termination of the spinal cord. It may be an isolated anomaly or be associated with other defects, including sacral agenesis, anorectal and genitourinary anomalies. The conus is not identifiable. The myelocystocele sac may have a significant lipomatous component (terminal lipomyelocystocele)."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17457,
      "label": "myelocystocele",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17449
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020966",
          "MEDGEN:1639659",
          "Orphanet:268813",
          "SCTID:203994003",
          "UMLS:C4551677",
          "icd11.foundation:863949070"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0017077"
    },
    {
      "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": 17457,
      "label": "myelocystocele"
    },
    {
      "id": 25974,
      "label": "saccular spinal dysraphism with a stalk to the dome"
    }
  ]
}