{
  "id": 16028,
  "label": "hereditary angioedema type 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015053",
  "properties": {
    "xrefs": [
      "GARD:0016933",
      "ICD9:279.8",
      "MEDGEN:403466",
      "Orphanet:100050",
      "SCTID:234619000",
      "UMLS:C2717906"
    ],
    "synonyms": [
      "HAE 1",
      "HAE-I",
      "hereditary angioneurotic edema type 1",
      "hereditary angioneurotic oedema type 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Hereditary angioedema type 1 (HAE 1) is a form of hereditary angioedema characterized by acute edema in subcutaneous tissues, viscera and/or the upper airway."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 22757,
      "label": "hereditary angioedema with C1Inh deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19413
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080939",
          "GARD:0022194",
          "MEDGEN:1812520",
          "OMIM:106100",
          "Orphanet:528623",
          "UMLS:C4552294"
        ],
        "synonyms": [
          "angioedema, hereditary, 1 and 2",
          "angioedema, hereditary, type 1/2",
          "C1 esterase inhibitor, deficiency of",
          "HAE1",
          "angioedema, hereditary, type 1",
          "angioedema, hereditary, type 2",
          "angioedema, hereditary, type I",
          "angioneurotic edema, hereditary"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Forms of hereditary angioedema that occur due to mutations in the gene for complement C1 inhibitor protein. Type I hereditary angioedema is associated with reduced serum levels of complement C1 inhibitor protein. Type II hereditary angioedema is associated with the production of a non-functional complement C1 inhibitor protein."
      },
      "child_count": 2,
      "reference_id": "MONDO:0033946"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 22757,
      "label": "hereditary angioedema with C1Inh deficiency"
    }
  ]
}