{
  "id": 9526,
  "label": "Hailey-Hailey disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008218",
  "properties": {
    "xrefs": [
      "DOID:0050429",
      "GARD:0006559",
      "MEDGEN:43100",
      "MESH:D016506",
      "NANDO:1200631",
      "NCIT:C82865",
      "NORD:1211",
      "OMIM:169600",
      "Orphanet:2841",
      "SCTID:79468000",
      "UMLS:C0085106",
      "icd11.foundation:818400628"
    ],
    "synonyms": [
      "Hailey-Hailey disease",
      "benign chronic familial pemphigus of Hailey-Hailey",
      "benign chronic pemphigus",
      "pemphigus, benign familial",
      "BCPM",
      "benign familial pemphigus",
      "familial benign chronic pemphigus",
      "familial benign pemphigus"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "Benign chronic familial pemphigus of Hailey-Hailey is characterized by rhagades mostly located in the armpits, inguinal and perineal folds (scrotum, vulva)."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 8070,
      "label": "pemphigus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19177
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9182",
          "EFO:1000749",
          "GARD:0007352",
          "ICD10CM:L10",
          "ICD10WHO:L10",
          "ICD9:694.4",
          "MEDGEN:45369",
          "MESH:D010392",
          "NANDO:1200228",
          "NCIT:C34909",
          "SCTID:65172003",
          "UMLS:C0030807",
          "Wikipedia:Pemphigus",
          "icd11.foundation:191659986"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Pemphigus is a group of rare autoimmune diseases that cause blistering of the skin and mucous membranes (mouth, nose, throat, eyes, and genitals).This conditioncan occur at any age, but often strikes people in middle or older age. Studies have shown that some populations may be at greater risk for certain types of pemphigus. For instance, people of Jewish descent and those from India, Southeast Europe, and the Middle East are at greater risk for pemphigus vulargis, while pemphigus foliaceus is more common in North America, Turkey, and South America. Pemphigus is a chronic disease which is best controlled by early diagnosis and treatment.Treatment includes steroids to reduce inflammation,drugs that suppress the immune system responseand antibiotics to treat associated infections. There are four main types of pemphigus: Pemphigus vulgaris Pemphigus foliaceus IgA pemphigus Paraneoplastic pemphigus"
      },
      "child_count": 6,
      "reference_id": "MONDO:0006594"
    },
    {
      "id": 19129,
      "label": "epidermal disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1842776",
          "Orphanet:79353",
          "UMLS:C5681492"
        ],
        "synonyms": [
          "epidermal disease",
          "rare epidermal disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A skin disease that involves the epidermis."
      },
      "child_count": 25,
      "reference_id": "MONDO:0019268"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MESH:D012873",
          "SCTID:239001006"
        ],
        "synonyms": [
          "disease, genetic skin",
          "diseases, genetic skin",
          "genetic skin disease",
          "genetic skin diseases",
          "genodermatosis",
          "skin disease, genetic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of skin disease that is caused by a modification of the individual's genome."
      },
      "child_count": 228,
      "reference_id": "MONDO:0100118"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8070,
      "label": "pemphigus"
    },
    {
      "id": 19129,
      "label": "epidermal disease"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}