{
  "id": 3392,
  "label": "meningocele",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001147",
  "properties": {
    "xrefs": [
      "DOID:1088",
      "HP:0002435",
      "MEDGEN:44356",
      "MESH:D008588",
      "NCIT:C101209",
      "NCIT:C105595",
      "Orphanet:93968",
      "SCTID:171131006",
      "UMLS:C0025299"
    ],
    "synonyms": [
      "central nervous system meningocele",
      "meningocele",
      "meningocele (disease)",
      "spinal meningocele"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A congenital abnormality in which the meninges protrude through a defect in the spinal column or the cranium."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 4427,
      "label": "congenital nervous system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2490",
          "ICD9:742",
          "MEDGEN:105425",
          "NCIT:C97172",
          "UMLS:C0497552"
        ],
        "synonyms": [
          "congenital abnormality of the nervous system",
          "congenital nervous system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An abnormality of the nervous system that is present at birth or detected in the neonatal period."
      },
      "child_count": 217,
      "reference_id": "MONDO:0002320"
    }
  ],
  "children": [
    {
      "id": 17459,
      "label": "meningoencephalocele",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3392,
        7209,
        17458
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020968",
          "MEDGEN:82743",
          "NANDO:2200813",
          "NCIT:C124517",
          "Orphanet:268820",
          "SCTID:52330001",
          "UMLS:C0266456"
        ],
        "synonyms": [
          "brain meninx cephalocele (disease)",
          "cephalocele (disease) of brain meninx",
          "meningoencephalocele",
          "cranial meningocele",
          "encephalomeningocele"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A congenital abnormality in which the meninges protrude through a defect in the cranium."
      },
      "child_count": 0,
      "reference_id": "MONDO:0017079"
    }
  ],
  "roots": [
    {
      "id": 4427,
      "label": "congenital nervous system disorder"
    }
  ]
}