{
  "id": 8067,
  "label": "panniculitis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0006591",
  "properties": {
    "xrefs": [
      "DOID:1526",
      "EFO:1000746",
      "ICD9:729.3",
      "ICD9:729.30",
      "ICD9:729.39",
      "MEDGEN:45301",
      "MESH:D015434",
      "NCIT:C33645",
      "SCTID:22125009",
      "UMLS:C0030326",
      "Wikipedia:Panniculitis",
      "icd11.foundation:1056888958"
    ],
    "synonyms": [
      "Subcutaneous adipose tissue",
      "Subcutaneous tissue",
      "inflammation of subcutaneous adipose tissue",
      "subcutaneous adipose tissue inflammation",
      "subcutis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      }
    ],
    "definition": "Inflammation of the subcutaneous adipose tissue."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 6,
  "parents": [
    {
      "id": 4198,
      "label": "integumentary system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:16",
          "EFO:0010285",
          "MEDGEN:712400",
          "SCTID:128598002",
          "UMLS:C1290011"
        ],
        "synonyms": [
          "disease of integumental system",
          "disease or disorder of integumental system",
          "disorder of integumental system",
          "integumental system disease",
          "integumental system disease or disorder",
          "integumentary disease",
          "disorder of integument"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A disease involving the integumental system."
      },
      "child_count": 36,
      "reference_id": "MONDO:0002051"
    },
    {
      "id": 5762,
      "label": "connective tissue disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:65",
          "EFO:1001986",
          "MEDGEN:1098",
          "MESH:D003240",
          "NANDO:2100172",
          "NCIT:C26729",
          "SCTID:105969002",
          "UMLS:C0009782"
        ],
        "synonyms": [
          "connective tissue disease",
          "connective tissue disease or disorder",
          "connective tissue diseases",
          "connective tissue disorder",
          "connective tissue disorders",
          "disease of connective tissue",
          "disease or disorder of connective tissue",
          "disease, connective tissue",
          "disorder of connective tissue",
          "primary disorder of connective tissue",
          "tissue disease, connective"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A disease involving the connective tissue."
      },
      "child_count": 16,
      "reference_id": "MONDO:0003900"
    },
    {
      "id": 20399,
      "label": "inflammatory disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29380
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD9:799.89",
          "MEDGEN:452939",
          "NCIT:C93210",
          "SCTID:128139000",
          "UMLS:C1290884"
        ],
        "synonyms": [
          "anatomical structure inflammation",
          "inflammation of anatomical structure",
          "inflammatory disease",
          "inflammatory disorder"
        ],
        "definition": "A disease involving a pathogenic inflammatory response in the anatomical structure."
      },
      "child_count": 94,
      "reference_id": "MONDO:0021166"
    }
  ],
  "children": [
    {
      "id": 18226,
      "label": "nodular non-suppurative panniculitis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8067,
        19144
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1525",
          "EFO:1000742",
          "GARD:0007879",
          "MEDGEN:10559",
          "MESH:D010201",
          "MedDRA:10047883",
          "Orphanet:33577",
          "SCTID:33760009",
          "UMLS:C0030328"
        ],
        "synonyms": [
          "Pfeiffer-Weber-Christian syndrome",
          "Relapsing febrile nodular nonsuppurative panniculitis",
          "Relapsing febrile nodular panniculitis",
          "WCD",
          "Weber-Christian disease",
          "Weber-Christian panniculitis",
          "idiopathic lobular panniculitis",
          "idiopathic nodular panniculitis",
          "nodular nonsuppurative panniculitis",
          "Weber Christian disease",
          "panniculitis nodular nonsuppurative"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "Nodular non-suppurative panniculitis, known as Weber-Christian disease (WCD), is a rare skin disorder characterized by recurring inflammation in the subcutaneous layer of fat."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018063"
    },
    {
      "id": 19362,
      "label": "panniculitis and localized lipodystrophy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8067,
        19064
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019128",
          "MEDGEN:1678538",
          "Orphanet:90159",
          "UMLS:C5190785"
        ],
        "synonyms": [
          "panniculitis-induced localised lipodystrophy",
          "panniculitis-induced localized lipodystrophy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0019555"
    },
    {
      "id": 19368,
      "label": "lupus erythematosus panniculitis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8067,
        16381
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019133",
          "MEDGEN:14589",
          "MESH:D015435",
          "NCIT:C82884",
          "Orphanet:90285",
          "SCTID:15084002",
          "UMLS:C0030327"
        ],
        "synonyms": [
          "lupus erythematosus profundus",
          "lupus panniculitis",
          "lupus profundus"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A type of lupus erythematosus characterized by deep dermal or subcutaneous nodules, most often on the head, face, or upper arms. It is generally chronic and occurs most often in women between the ages of 20 and 45."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019561"
    },
    {
      "id": 19532,
      "label": "cytophagic histiocytic panniculitis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8067,
        19144
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019249",
          "MEDGEN:590528",
          "Orphanet:94087",
          "SCTID:238883003",
          "UMLS:C0406594",
          "icd11.foundation:1978274002"
        ],
        "synonyms": [
          "CHP",
          "Winkelmann cytophagic panniculitis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "Cytophagic histiocytic panniculitis (CHP) is a very rare form of panniculitis manifesting as recurrent multiple subcutaneous nodules (which may progressively become ecchymotic and ulcerated), and histologically characterized by lobular panniculitis with lymphocytic and histiocytic infiltration in the subcutaneous adipose tissue."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019789"
    },
    {
      "id": 21255,
      "label": "lipodermatosclerosis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4496,
        8067,
        19369
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009671",
          "MEDGEN:140802",
          "MESH:C537026",
          "SCTID:410016009",
          "UMLS:C0406500",
          "icd11.foundation:473315619"
        ],
        "synonyms": [
          "acute lipodermatosclerosis",
          "hypodermitis sclerodermaformis",
          "sclerosing panniculitis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "Lipodermatosclerosis refers to changes in the skin of the lower legs. It is a form of panniculitis (inflammation of the layer of fat under the skin). Signs and symptoms include pain, hardening of skin, change in skin color (redness), swelling, and a tapering of the legs above the ankles. The exact underlying cause is unknown; however, it appears to be associated with venous insufficiency and/or obesity. Treatment usually includes compression therapy."
      },
      "child_count": 0,
      "reference_id": "MONDO:0023646"
    },
    {
      "id": 25180,
      "label": "erythema nodosum",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8067
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080750",
          "ICD10CM:L52",
          "ICD10WHO:L52",
          "MEDGEN:41858",
          "UMLS:C0014743",
          "icd11.foundation:1628519266"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A panniculitis that is characterized by sudden onset of painful, erythematous, subcutaneous nodules mainly localized to the pretibial areas. Lesions are usually bilateral and symmetrical, ranging from 1 to 5 cm in diameter."
      },
      "child_count": 0,
      "reference_id": "MONDO:0850231"
    }
  ],
  "roots": [
    {
      "id": 4198,
      "label": "integumentary system disorder"
    },
    {
      "id": 5762,
      "label": "connective tissue disorder"
    },
    {
      "id": 20399,
      "label": "inflammatory disease"
    }
  ]
}