{
  "id": 9080,
  "label": "TNF receptor 1-associated periodic fever syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007727",
  "properties": {
    "xrefs": [
      "DOID:0090018",
      "GARD:0008457",
      "MEDGEN:226899",
      "MESH:C536657",
      "NANDO:1200472",
      "NANDO:2200433",
      "NCIT:C119051",
      "NORD:1804",
      "OMIM:142680",
      "Orphanet:32960",
      "SCTID:403833009",
      "UMLS:C1275126",
      "icd11.foundation:1869883509"
    ],
    "synonyms": [
      "autosomal dominant familial periodic fever",
      "FHF",
      "Hibernian fever, familial",
      "TNF receptor 1-associated periodic fever syndrome",
      "TNF receptor 1-associated periodic syndrome",
      "TNF receptor-associated periodic syndrome",
      "TRAPS",
      "TRAPS syndrome",
      "Tumor Necrosis Factor Receptor-Associated Periodic Syndrome",
      "familial Hibernian fever",
      "tumor necrosis factor receptor 1 associated periodic syndrome",
      "tumor necrosis factor receptor 1-associated periodic syndrome",
      "tumor necrosis factor receptor-associated periodic syndrome",
      "tumour necrosis factor receptor 1 associated periodic syndrome",
      "tumour necrosis factor receptor 1-associated periodic syndrome",
      "tumour necrosis factor receptor-associated periodic syndrome",
      "FPF",
      "periodic FEVER, familial, autosomal dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "A periodic fever syndrome, characterized by recurrent fever, arthralgia, myalgia and tender skin lesions lasting for 1 to 3 weeks, associated with skin, joint, ocular and serosal inflammation and complicated by secondary amyloidosis."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6778,
      "label": "immune system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2914",
          "EFO:0000540",
          "ICD9:279",
          "ICD9:279.1",
          "ICD9:279.10",
          "ICD9:279.19",
          "ICD9:279.4",
          "ICD9:279.49",
          "ICD9:279.8",
          "ICD9:279.9",
          "MEDGEN:5759",
          "MESH:D007154",
          "NANDO:1100004",
          "NANDO:2100202",
          "NCIT:C3507",
          "SCTID:414029004",
          "UMLS:C0021053"
        ],
        "synonyms": [
          "disease of immune system",
          "disease or disorder of immune system",
          "disorder of immune system",
          "immune disease",
          "immune disorder",
          "immune dysfunction",
          "immune system disease or disorder",
          "immune system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A disorder resulting from an abnormality in the immune system."
      },
      "child_count": 47,
      "reference_id": "MONDO:0005046"
    },
    {
      "id": 18150,
      "label": "hereditary periodic fever syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16077,
        21247
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021453",
          "MEDGEN:199651",
          "MESH:D056660",
          "Orphanet:324924",
          "UMLS:C0751422"
        ],
        "synonyms": [
          "hereditary periodic fever syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "An instance of periodic fever syndrome that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 12,
      "reference_id": "MONDO:0017953"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6778,
      "label": "immune system disorder"
    },
    {
      "id": 18150,
      "label": "hereditary periodic fever syndrome"
    }
  ]
}