{
  "id": 13574,
  "label": "hereditary angioedema type 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012526",
  "properties": {
    "xrefs": [
      "DOID:0080940",
      "GARD:0016935",
      "ICD9:277.6",
      "MEDGEN:346653",
      "MESH:D056828",
      "OMIM:610618",
      "Orphanet:100054",
      "SCTID:427167008",
      "UMLS:C1857728"
    ],
    "synonyms": [
      "F12 hereditary angioedema",
      "HAE 3",
      "HAE-III",
      "angioedema, hereditary, 3",
      "hereditary angioedema caused by mutation in F12",
      "hereditary angioedema type 3",
      "hereditary angioneurotic edema type 3",
      "hereditary angioneurotic oedema type 3",
      "inherited estrogen-associated angioedema",
      "inherited estrogen-associated angioneurotic edema",
      "inherited estrogen-associated angioneurotic oedema",
      "inherited estrogen-dependent angioedema",
      "inherited estrogen-dependent angioneurotic edema",
      "inherited estrogen-dependent angioneurotic oedema",
      "HAE3",
      "Hae 3",
      "Hae with normal C1 inhibitor concentration and function",
      "angioedema, hereditary, type 3",
      "angioedema, hereditary, type III",
      "angioneurotic edema, hereditary, with normal C1 inhibitor concentration and function",
      "estrogen-related Hae",
      "estrogen-sensitive Hae",
      "hereditary angioedema with normal C1 inhibitor activity"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Hereditary angioedema type 3 (HAE 3) 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": 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"
    }
  ]
}