{
  "id": 11639,
  "label": "angioedema",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010481",
  "properties": {
    "xrefs": [
      "CSP:2716-7007",
      "DOID:1558",
      "EFO:0005532",
      "HP:0100665",
      "ICD9:995.1",
      "MEDGEN:1543",
      "MESH:D000799",
      "SCTID:400075008",
      "UMLS:C0002994"
    ],
    "synonyms": [
      "Edemas, angioneurotic",
      "Quincke edema",
      "Quincke oedema",
      "Quincke's edema",
      "Quincke's oedema",
      "Quinckes edema",
      "Quinckes oedema",
      "Urticarias, giant",
      "angioedemas",
      "angioneurotic Edemas",
      "edema, Quincke's",
      "edema, angioneurotic",
      "giant Urticarias",
      "giant urticaria",
      "urticaria, giant",
      "angioneurotic edema",
      "angioneurotic oedema"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Swelling involving the deep dermis, subcutaneous, or submucosal tissues, representing localized edema. Angioedema often occurs in the face, lips, tongue, and larynx."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 7148,
      "label": "urticaria",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4496
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1555",
          "EFO:0005531",
          "HP:0001025",
          "ICD10CM:L50",
          "ICD10WHO:L50",
          "ICD9:708",
          "ICD9:708.8",
          "ICD9:708.9",
          "MEDGEN:22587",
          "MESH:D014581",
          "NCIT:C3432",
          "SCTID:126485001",
          "UMLS:C0042109"
        ],
        "synonyms": [
          "hives",
          "urticaria",
          "urticaria (disease)",
          "Urticarias"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A vascular reaction of the skin characterized by erythema and wheal formation due to localized increase of vascular permeability. The causative mechanism may be allergy, infection, or stress."
      },
      "child_count": 14,
      "reference_id": "MONDO:0005492"
    },
    {
      "id": 19142,
      "label": "skin vascular disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6820,
        7065
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9540",
          "ICD9:709.1",
          "MEDGEN:102473",
          "MESH:D017445",
          "MedDRA:10062171",
          "NCIT:C35254",
          "Orphanet:79379",
          "SCTID:11263005",
          "UMLS:C0162819"
        ],
        "synonyms": [
          "skin vascular disorder",
          "superficial vasculature disease",
          "vascular disease of the skin",
          "vascular skin disease",
          "vasculature skin disease",
          "disorder of blood vessels affecting skin",
          "vascular disorder of skin",
          "vascular disorders of skin"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A disease that involves the superficial vasculature."
      },
      "child_count": 40,
      "reference_id": "MONDO:0019293"
    }
  ],
  "children": [
    {
      "id": 18928,
      "label": "non-histaminic angioedema",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8013,
        11639
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018701",
          "ICD9:995.1",
          "Orphanet:658",
          "SCTID:41291007"
        ],
        "synonyms": [
          "angioneurotic edema",
          "angioneurotic oedema",
          "bradykinine-induced angioedema",
          "non histamine-induced angioedema"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Angioedema is characterized by the occurrence of transitory and recurrent subcutaneous and/or submucosal edemas resulting in swelling and/or abdominal pain."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019013"
    },
    {
      "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"
    },
    {
      "id": 19414,
      "label": "acquired angioedema",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        11639
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080941",
          "GARD:0008605",
          "MEDGEN:419486",
          "MESH:C538173",
          "Orphanet:91385",
          "UMLS:C2931758",
          "icd11.foundation:1078767412"
        ],
        "synonyms": [
          "AAE",
          "acquired C1 inhibitor deficiency",
          "acquired angioedema",
          "acquired angioneurotic edema",
          "acquired angioneurotic oedema",
          "acquired bradykinine-induced angioedema",
          "acquired non histamine-induced angioedema",
          "angioedema, acquired"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Acquired angioedema (AAE) is characterized by the occurrence of transitory and recurrent subcutaneous and/or submucosal edemas resulting in swelling and/or abdominal pain due to an acquired C1 inhibitor (C1-INH) deficiency."
      },
      "child_count": 5,
      "reference_id": "MONDO:0019624"
    }
  ],
  "roots": [
    {
      "id": 7148,
      "label": "urticaria"
    },
    {
      "id": 19142,
      "label": "skin vascular disease"
    }
  ]
}