{
  "id": 25858,
  "label": "epidermolytic hyperkeratosis 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0958184",
  "properties": {
    "xrefs": [
      "DOID:0081359",
      "GARD:0026961"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 8644,
      "label": "epidermolytic ichthyosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17595,
        23507
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4603",
          "GARD:0024537",
          "MEDGEN:38179",
          "MESH:D017488",
          "NORD:1100",
          "OMIMPS:113800",
          "SCTID:254167000",
          "UMLS:C0079153",
          "icd11.foundation:1183730789"
        ],
        "synonyms": [
          "BCIE",
          "EHK",
          "EI",
          "bullous congenital ichthyosiform erythroderma",
          "bullous congenital ichthyosiform erythroderma of Brock",
          "bullous ichthyosis",
          "epidermolytic hyperkeratosis",
          "epidermolytic ichthyosis",
          "ichthyosis hystrix Brocq type",
          "autosomal dominant epidermolytic ichthyosis",
          "bullous erythroderma Ichthyosiformis congenita of Brocq",
          "bullous ichthyosiform erythroderma",
          "bullous ichthyosiform erythroderma congenita",
          "congenital bullous ichthyosiform erythroderma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A rare keratinopathic ichthyosis (KPI), that is characterized by a blistering phenotype at birth which progressively becomes hyperkeratotic."
      },
      "child_count": 8,
      "reference_id": "MONDO:0007239"
    }
  ],
  "children": [
    {
      "id": 24039,
      "label": "ichthyosis, annular epidermolytic 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        12949,
        25858
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015417",
          "OMIM:607602"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Any annular epidermolytic ichthiosis in which the cause of the disease is a variation in the KRT10 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0100303"
    },
    {
      "id": 24640,
      "label": "epidermolytic hyperkeratosis 2B, autosomal recessive",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        23417,
        25858
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061208",
          "GARD:0026394",
          "MEDGEN:1845041",
          "OMIM:620707",
          "UMLS:C5882753"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0700245"
    },
    {
      "id": 24643,
      "label": "epidermolytic hyperkeratosis 2A, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20109,
        25858
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061223",
          "GARD:0026396",
          "MEDGEN:1846123",
          "OMIM:620150",
          "UMLS:C5882671"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0700248"
    }
  ],
  "roots": [
    {
      "id": 8644,
      "label": "epidermolytic ichthyosis"
    }
  ]
}