{
  "id": 15348,
  "label": "white sponge nevus 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014346",
  "properties": {
    "xrefs": [
      "DOID:0081288",
      "GARD:0016012",
      "MEDGEN:862758",
      "OMIM:615785",
      "UMLS:C4014321"
    ],
    "synonyms": [
      "White sponge Nevus type 2",
      "white sponge nevus 2",
      "WHITE sponge NEVUS 2",
      "WSN2"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16507,
      "label": "hereditary mucosal leukokeratosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6801,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050448",
          "GARD:0008501",
          "ICD9:528.6",
          "MEDGEN:328433",
          "MESH:D053529",
          "NCIT:C84760",
          "OMIMPS:193900",
          "Orphanet:171723",
          "SCTID:389203001",
          "UMLS:C1721005"
        ],
        "synonyms": [
          "White sponge nevus of Cannon",
          "hereditary mucosal leukokeratosis",
          "white sponge nevus",
          "white sponge nevus of Cannon"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "White sponge nevus (WSN) is a rare and autosomal dominant genetic disease in which the oral mucosa is white or grayish, thickened, folded, and spongy. The onset is early in life, and both sexes are affected equally. Other common sites include the tongue, floor of the mouth, and alveolar mucosa."
      },
      "child_count": 4,
      "reference_id": "MONDO:0015748"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16507,
      "label": "hereditary mucosal leukokeratosis"
    }
  ]
}