{
  "id": 19300,
  "label": "subcutaneous panniculitis-like T-cell lymphoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019475",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3028,
      "label": "immune system cancer",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6733,
        6778
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060083"
        ],
        "synonyms": [
          "cancer of immune system",
          "immune system cancer",
          "malignant immune system neoplasm",
          "malignant neoplasm of immune system"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A malignant neoplasm involving the immune system"
      },
      "child_count": 50,
      "reference_id": "MONDO:0000621"
    },
    {
      "id": 6569,
      "label": "leukocyte disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6778,
        7217
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9500",
          "ICD9:288",
          "ICD9:288.9",
          "MEDGEN:7325",
          "MESH:D007960",
          "SCTID:54097007",
          "UMLS:C0023510"
        ],
        "synonyms": [
          "disease of leukocyte",
          "disease or disorder of leukocyte",
          "disorder of leukocyte",
          "disorder, leukocyte",
          "disorders, leukocyte",
          "leukocyte disease",
          "leukocyte disease or disorder",
          "leukocyte disorder",
          "white blood cell disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "A disease involving leukocytes."
      },
      "child_count": 46,
      "reference_id": "MONDO:0004805"
    },
    {
      "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"
    },
    {
      "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": [],
  "roots": [
    {
      "id": 3028,
      "label": "immune system cancer"
    },
    {
      "id": 6569,
      "label": "leukocyte disorder"
    },
    {
      "id": 16568,
      "label": "indolent primary cutaneous T-cell lymphoma"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}