{
  "id": 18825,
  "label": "primary cutaneous CD30+ T-cell lymphoproliferative disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018897",
  "properties": {
    "xrefs": [
      "GARD:0018697",
      "MEDGEN:1843249",
      "MedDRA:10065863",
      "NCIT:C7195",
      "Orphanet:541",
      "UMLS:C5679826",
      "icd11.foundation:1046496266"
    ],
    "synonyms": [
      "primary cutaneous Ki-1+ T-cell lymphoproliferative disease"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 16568,
      "label": "indolent primary cutaneous T-cell lymphoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16515
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020161",
          "MEDGEN:1843370",
          "Orphanet:178548",
          "UMLS:C5680498"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0015816"
    }
  ],
  "children": [
    {
      "id": 17878,
      "label": "primary cutaneous anaplastic large cell lymphoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3019,
        18825,
        19798,
        20048
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021247",
          "MEDGEN:266255",
          "MESH:D054446",
          "MedDRA:10065863",
          "NCIT:C6860",
          "ONCOTREE:PCALCL",
          "Orphanet:300865",
          "UMLS:C1301362",
          "icd11.foundation:1972636482"
        ],
        "synonyms": [
          "ALCL, cutaneous",
          "C-ALCL",
          "anaplastic large-cell lymphoma, primary cutaneous type",
          "primary C-ALCL",
          "primary anaplastic large cell lymphoma of skin",
          "primary anaplastic large cell lymphoma of the skin",
          "primary cutaneous CD30 Positive anaplastic large cell lymphoma",
          "primary cutaneous CD30+ ALCL",
          "primary cutaneous CD30+ anaplastic large cell lymphoma",
          "regressive atypical histiocytosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Primary cutaneous anaplastic large cell lymphoma (C-ALCL) is a rare T-cell non-Hodgkin lymphoma that affects the skin and generally shows no extracutaneous involvement at presentation. It belongs to the spectrum of primary cutaneous CD30+ lymphoproliferative disorders along with lymphomatoid papulosis with which it shares overlapping clinical and histopathologic features."
      },
      "child_count": 0,
      "reference_id": "MONDO:0017598"
    },
    {
      "id": 19799,
      "label": "lymphomatoid papulosis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18825
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0006944",
          "ICD9:447.8",
          "ICDO:9718/1",
          "MEDGEN:61534",
          "MESH:D017731",
          "MedDRA:10056670",
          "NCIT:C3721",
          "ONCOTREE:LYP",
          "Orphanet:98842",
          "SCTID:31047003",
          "UMLS:C0206182",
          "icd11.foundation:1791207220"
        ],
        "synonyms": [
          "LyP",
          "LYP"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Lymphomatoid papulosis (LyP) is a rare cutaneous condition characterized by chronic, recurrent, and self-regressing papulonodular skin eruptions. It belongs to the spectrum of primary cutaneous CD30+ lymphoproliferative disorders, along with primary cutaneous anaplastic large cell lymphoma (primary C-ALCL) with which it shares overlapping clinical and histopathologic features."
      },
      "child_count": 0,
      "reference_id": "MONDO:0020326"
    }
  ],
  "roots": [
    {
      "id": 16568,
      "label": "indolent primary cutaneous T-cell lymphoma"
    }
  ]
}