{
  "id": 21260,
  "label": "angioedema, hereditary, 6",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0023660",
  "properties": {
    "xrefs": [
      "GARD:0025373",
      "MEDGEN:1785484",
      "OMIM:619363",
      "UMLS:C5543516"
    ],
    "synonyms": [
      "HAE6"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19413,
      "label": "hereditary angioedema",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        11639,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:14735",
          "GARD:0005979",
          "MEDGEN:9229",
          "MESH:D054179",
          "MedDRA:10019860",
          "NANDO:1200365",
          "NANDO:2200795",
          "NCIT:C84758",
          "OMIMPS:106100",
          "Orphanet:91378",
          "SCTID:82966003",
          "UMLS:C0019243",
          "icd11.foundation:795969334"
        ],
        "synonyms": [
          "HAE",
          "familial angioneurotic edema",
          "familial angioneurotic oedema",
          "hereditary angioedema",
          "hereditary angioneurotic edema",
          "hereditary angioneurotic oedema",
          "hereditary bradykinine-induced angioedema",
          "hereditary non histamine-induced angioedema",
          "angioedema, hereditary",
          "deficiency of C1 esterase inhibitor"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Hereditary angioedema (HAE) is a genetic disease characterized by the occurrence of transitory and recurrent subcutaneous and/or submucosal edemas resulting in swelling and/or abdominal pain."
      },
      "child_count": 20,
      "reference_id": "MONDO:0019623"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19413,
      "label": "hereditary angioedema"
    }
  ]
}