{
  "id": 24640,
  "label": "epidermolytic hyperkeratosis 2B, autosomal recessive",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0700245",
  "properties": {
    "xrefs": [
      "DOID:0061208",
      "GARD:0026394",
      "MEDGEN:1845041",
      "OMIM:620707",
      "UMLS:C5882753"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 23417,
      "label": "autosomal recessive epidermolytic ichthyosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7611,
        8644
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022074",
          "MEDGEN:1725198",
          "NANDO:1200612",
          "NANDO:2200989",
          "Orphanet:512103",
          "UMLS:C5437635",
          "icd11.foundation:244597687"
        ],
        "synonyms": [
          "AREI"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0044742"
    },
    {
      "id": 25858,
      "label": "epidermolytic hyperkeratosis 2",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
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      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081359",
          "GARD:0026961"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0958184"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23417,
      "label": "autosomal recessive epidermolytic ichthyosis"
    },
    {
      "id": 25858,
      "label": "epidermolytic hyperkeratosis 2"
    }
  ]
}