{
  "id": 20803,
  "label": "Boerhaave syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0022013",
  "properties": {
    "xrefs": [
      "MEDGEN:65948",
      "MESH:C536571",
      "SCTID:19995004",
      "UMLS:C0238115"
    ],
    "synonyms": [
      "Boerhaave syndrome",
      "spontaneous rupture of esophagus",
      "spontaneous rupture of oesophagus",
      "Boerhaave's syndrome",
      "Boerhave syndrome",
      "boerhaave's syndrome",
      "spontaneous esophageal perforation",
      "spontaneous perforation of esophagus",
      "spontaneous perforation of oesophagus",
      "spontaneous perforation of the esophagus",
      "spontaneous perforation of the oesophagus",
      "spontaneous rupture of the esophagus",
      "spontaneous rupture of the oesophagus"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "A syndrome characterized by spontaneous longitudinal transmural rupture of the esophagus, usually in its distal part."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    }
  ]
}