{
  "id": 16568,
  "label": "indolent primary cutaneous T-cell lymphoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015816",
  "properties": {
    "xrefs": [
      "GARD:0020161",
      "MEDGEN:1843370",
      "Orphanet:178548",
      "UMLS:C5680498"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 4,
  "parents": [
    {
      "id": 16515,
      "label": "primary cutaneous T-cell lymphoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16517,
        18826
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0006226",
          "MEDGEN:36336",
          "MedDRA:10011677",
          "Orphanet:171901",
          "UMLS:C0079773"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 8,
      "reference_id": "MONDO:0015758"
    }
  ],
  "children": [
    {
      "id": 16563,
      "label": "primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16568
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020156",
          "MEDGEN:1842165",
          "Orphanet:178522",
          "UMLS:C5680503"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0015810"
    },
    {
      "id": 16571,
      "label": "mycosis fungoides and variants",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16568
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020166",
          "Orphanet:178566",
          "icd11.foundation:2036068731"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Mycosis fungoides (MF) and its variants represent the most common forms of cutaneous T-cell lymphomas. The term MF is restricted to the classical form characterized by the slow progression of patches, plaques and tumors, and to variants with a similar indolent course."
      },
      "child_count": 2,
      "reference_id": "MONDO:0015821"
    },
    {
      "id": 18825,
      "label": "primary cutaneous CD30+ T-cell lymphoproliferative disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16568
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0018897"
    },
    {
      "id": 19300,
      "label": "subcutaneous panniculitis-like T-cell lymphoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3028,
        6569,
        16568,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070662",
          "EFO:1000552",
          "GARD:0010193",
          "ICD10CM:C86.3",
          "ICD9:202.70",
          "ICDO:9708/3",
          "MEDGEN:99306",
          "MESH:C537503",
          "NANDO:2200030",
          "NCIT:C6918",
          "OMIM:618398",
          "ONCOTREE:SPTCL",
          "Orphanet:86884",
          "SCTID:404133000",
          "UMLS:C0522624",
          "icd11.foundation:1550338805"
        ],
        "synonyms": [
          "SPTCL",
          "subcutaneous panniculitic T-cell lymphoma",
          "subcutaneous panniculitis-like T-cell lymphoma",
          "subcutaneous panniculitis-like T-cell lymphoma (Alpha/Beta type)",
          "subcutaneous panniculitis-like T-cell lymphoma, Alpha/Beta type",
          "T-CELL LYMPHOMA, SUBCUTANEOUS PANNICULITIS-LIKE"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare cytotoxic cutaneous lymphoma that has been recognized as a distinct subset of peripheral T-cell lymphomas originating and presenting primarily in the subcutaneous fat tissue."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019475"
    }
  ],
  "roots": [
    {
      "id": 16515,
      "label": "primary cutaneous T-cell lymphoma"
    }
  ]
}