{
  "id": 14033,
  "label": "dyschromatosis universalis hereditaria 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012993",
  "properties": {
    "xrefs": [
      "GARD:0015581",
      "MEDGEN:382542",
      "MESH:C567194",
      "OMIM:612715",
      "UMLS:C2675183"
    ],
    "synonyms": [
      "dyschromatosis universalis hereditaria 2",
      "DUH2"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3112,
      "label": "dyschromatosis universalis hereditaria",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19140,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060304",
          "GARD:0001996",
          "MEDGEN:419691",
          "MESH:C535730",
          "NCIT:C173131",
          "OMIMPS:127500",
          "Orphanet:241",
          "SCTID:239082002",
          "UMLS:C2930995",
          "icd11.foundation:480710406"
        ],
        "synonyms": [
          "dyschromatosis universalis",
          "DUH"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution."
      },
      "child_count": 6,
      "reference_id": "MONDO:0000736"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3112,
      "label": "dyschromatosis universalis hereditaria"
    }
  ]
}