{
  "id": 17457,
  "label": "myelocystocele",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017077",
  "properties": {
    "xrefs": [
      "GARD:0020966",
      "MEDGEN:1639659",
      "Orphanet:268813",
      "SCTID:203994003",
      "UMLS:C4551677",
      "icd11.foundation:863949070"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 17449,
      "label": "spina bifida cystica",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19188
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020958",
          "MEDGEN:21277",
          "MESH:D016137",
          "MedDRA:10071011",
          "NANDO:1200509",
          "NANDO:2100215",
          "NANDO:2200814",
          "NCIT:C101201",
          "Orphanet:268744",
          "UMLS:C0037917",
          "icd11.foundation:979482551"
        ],
        "synonyms": [
          "meningomyelocele",
          "myelomeningocele",
          "open spina bifida",
          "spina bifida aperta",
          "spina bifida manifesta",
          "spina bifida, open"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A congenital abnormality in which the spinal cord and meninges protrude through a defect in the spinal column. The protrusion is above the skin surface."
      },
      "child_count": 5,
      "reference_id": "MONDO:0017069"
    }
  ],
  "children": [
    {
      "id": 25677,
      "label": "non-terminal myelocystocele",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17457
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026832",
          "MEDGEN:1843415",
          "Orphanet:645340",
          "UMLS:C5816719"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare closed spinal dysraphism characterized by myelocystocele located above the conus region. Also considered as a form of saccular limited dorsal myeloschisis."
      },
      "child_count": 0,
      "reference_id": "MONDO:0957451"
    },
    {
      "id": 25989,
      "label": "terminal myelocystocele",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17457,
        25974
      ],
      "type_id": 0,
      "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)."
      },
      "child_count": 0,
      "reference_id": "MONDO:0970962"
    }
  ],
  "roots": [
    {
      "id": 17449,
      "label": "spina bifida cystica"
    }
  ]
}