{
  "id": 15305,
  "label": "dowling-degos disease 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014301",
  "properties": {
    "xrefs": [
      "GARD:0016001",
      "MEDGEN:816616",
      "OMIM:615674",
      "UMLS:C3810286"
    ],
    "synonyms": [
      "DDD3",
      "Dowling-Degos disease 3"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9670,
      "label": "Dowling-Degos disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2731,
        17976,
        19140
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060256",
          "GARD:0009775",
          "MEDGEN:811363",
          "MESH:C562924",
          "MedDRA:10068651",
          "Orphanet:79145",
          "UMLS:C3714534",
          "icd11.foundation:15123132"
        ],
        "synonyms": [
          "Dowling-Degos disease type 1",
          "reticular pigment anomaly of flexures",
          "DDD1",
          "Dowling-Degos Kitamura disease",
          "Dowling-Degos disease 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A pigmentation disease characterized by a reticulate pattern of abnormally dark skin coloring, particularly in the body's folds and creases."
      },
      "child_count": 12,
      "reference_id": "MONDO:0008371"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9670,
      "label": "Dowling-Degos disease"
    }
  ]
}