{
  "id": 9715,
  "label": "seborrheic keratosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008420",
  "properties": {
    "xrefs": [
      "DOID:6498",
      "EFO:0005584",
      "ICD10CM:L82",
      "ICD9:702.1",
      "MEDGEN:5957",
      "MESH:D017492",
      "NCIT:C9006",
      "OMIM:182000",
      "SCTID:398838000",
      "UMLS:C0022603",
      "Wikipedia:Seborrheic_keratosis"
    ],
    "synonyms": [
      "basal cell papilloma",
      "keratosis Seborrheica",
      "keratosis, seborrheic, somatic",
      "keratosis, seborrheic"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "A common benign skin neoplasm usually affecting older individuals. The lesions usually are multiple and arise in the face, chest, and shoulders. They appear as black or brown, slightly elevated skin lesions."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "parents": [
    {
      "id": 8047,
      "label": "keratosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6820,
        23507
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:161",
          "EFO:1000720",
          "MEDGEN:9625",
          "MESH:D007642",
          "NCIT:C34745",
          "SCTID:254666005",
          "UMLS:C0022593"
        ],
        "synonyms": [
          "keratoderma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A skin disorder consisting of hypertrophy of the stratum corneum of the skin."
      },
      "child_count": 18,
      "reference_id": "MONDO:0006566"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MESH:D012873",
          "SCTID:239001006"
        ],
        "synonyms": [
          "disease, genetic skin",
          "diseases, genetic skin",
          "genetic skin disease",
          "genetic skin diseases",
          "genodermatosis",
          "skin disease, genetic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of skin disease that is caused by a modification of the individual's genome."
      },
      "child_count": 228,
      "reference_id": "MONDO:0100118"
    }
  ],
  "children": [
    {
      "id": 3565,
      "label": "inflamed seborrheic keratosis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9715
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11685",
          "ICD10CM:L82.0",
          "ICD9:702.11",
          "MEDGEN:580965",
          "SCTID:442348004",
          "UMLS:C0376117"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0001337"
    },
    {
      "id": 8044,
      "label": "inverted follicular keratosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        9715
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:6945",
          "EFO:1000717",
          "ICD9:264.8",
          "MEDGEN:87190",
          "NCIT:C9007",
          "SCTID:394728005",
          "UMLS:C0334019",
          "Wikipedia:Inverted_follicular_keratosis",
          "icd11.foundation:2109084329"
        ],
        "synonyms": [
          "inverted follicular keratosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Seborrheic keratosis that arises from follicular structures in the skin. It presents as a solitary nodule in the skin and is characterized by the presence of prominent squamous eddies."
      },
      "child_count": 1,
      "reference_id": "MONDO:0006563"
    },
    {
      "id": 8058,
      "label": "melanoacanthoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9715
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11684",
          "EFO:1000733",
          "MEDGEN:272110",
          "NCIT:C27548",
          "SCTID:394727000",
          "UMLS:C1321683",
          "Wikipedia:Melanocanthoma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A benign, darkly pigmented skin lesion characterized by proliferation of keratinocytes and melanocytes."
      },
      "child_count": 0,
      "reference_id": "MONDO:0006579"
    },
    {
      "id": 8097,
      "label": "vulvar seborrheic keratosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4318,
        4707,
        6931,
        9715
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:6944",
          "GARD:0024446",
          "MEDGEN:237055",
          "NCIT:C6375",
          "UMLS:C1336981"
        ],
        "synonyms": [
          "mammalian vulva seborrheic keratosis",
          "seborrheic keratosis of mammalian vulva",
          "seborrheic keratosis of the vulva",
          "seborrheic keratosis of vulva"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "A benign squamous neoplasm that arises from the vulva. It is characterized by the proliferation of the basal cells in the squamous epithelium, acanthosis, hyperkeratosis, and cysts formation."
      },
      "child_count": 4,
      "reference_id": "MONDO:0006622"
    },
    {
      "id": 20683,
      "label": "eyelid seborrheic keratosis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5315,
        9715
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:137912",
          "NCIT:C4356",
          "SCTID:231826004",
          "UMLS:C0339109"
        ],
        "synonyms": [
          "basal cell papilloma of eyelid",
          "basal cell papilloma of the eyelid",
          "eyelid basal cell papilloma",
          "eyelid seborrheic keratosis",
          "seborrheic keratosis of eyelid",
          "seborrheic keratosis of the eyelid"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A seborrheic keratosis that involves the eyelid."
      },
      "child_count": 0,
      "reference_id": "MONDO:0021607"
    }
  ],
  "roots": [
    {
      "id": 8047,
      "label": "keratosis"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}