{
  "id": 10425,
  "label": "junctional epidermolysis bullosa Herlitz type",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009182",
  "properties": {
    "xrefs": [
      "DOID:0060737",
      "GARD:0002153",
      "ICD10CM:Q81.1",
      "MEDGEN:36328",
      "NANDO:1201065",
      "NANDO:2200119",
      "NANDO:2201378",
      "OMIM:226700",
      "Orphanet:79404",
      "SCTID:400140006",
      "UMLS:C0079683"
    ],
    "synonyms": [
      "Herlitz-Pearson-type epidermolysis bullosa",
      "JEB, generalised severe",
      "JEB, generalized severe",
      "JEB-H",
      "JEB-Herlitz type",
      "epidermolysis bullosa letalis",
      "junctional epidermolysis bullosa generalisata gravis",
      "junctional epidermolysis bullosa, Herlitz-Pearson type",
      "Herlitz-Pearson type epidermolysis bullosa",
      "epidermolysis bullosa Junctionalis, Herlitz type",
      "epidermolysis bullosa, junctional, Herlitz type",
      "epidermolysis bullosa, junctional, Herlitz-Pearson type",
      "junctional epidermolysis bullosa, Herlitz type",
      "junctional epidermolysis bullosa, generalised severe",
      "junctional epidermolysis bullosa, generalized severe"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Junctional epidermolysis bullosa, Herlitz-type is a severe subtype of junctional epidermolysis bullosa (JEB) characterized by blisters and extensive erosions, localized to the skin and mucous membranes."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17889,
      "label": "junctional epidermolysis bullosa",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19133
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3209",
          "GARD:0002152",
          "MEDGEN:86898",
          "MESH:D016109",
          "NANDO:1200236",
          "NANDO:2201342",
          "NCIT:C90598",
          "OMIMPS:226650",
          "Orphanet:305",
          "SCTID:79855003",
          "UMLS:C0079301",
          "icd11.foundation:1501260457"
        ],
        "synonyms": [
          "EBJ",
          "JEB",
          "epidermolysis bullosa atrophicans",
          "junctional epidermolysis bullosa",
          "epidermolysis bullosa hereditaria letalis",
          "epidermolysis bullosa, junctional"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Junctional epidermolysis bullosa (JEB) is a form of inherited epidermolysis bullosa characterized by involvement of the skin and mucous membranes, and is defined by the formation of blistering lesions between the epidermis and the dermis at the lamina lucida level of the cutaneous basement membrane zone and by healing of lesions with atrophy and/or exuberant granulation tissue formation."
      },
      "child_count": 15,
      "reference_id": "MONDO:0017612"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17889,
      "label": "junctional epidermolysis bullosa"
    }
  ]
}