{
  "id": 11052,
  "label": "hyperimmunoglobulinemia D with periodic fever",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009849",
  "properties": {
    "xrefs": [
      "DOID:0081450",
      "GARD:0002788",
      "MEDGEN:140768",
      "NANDO:1200866",
      "NANDO:2200436",
      "OMIM:260920",
      "Orphanet:343",
      "UMLS:C0398691"
    ],
    "synonyms": [
      "HIDS",
      "hyper-IgD syndrome",
      "hyperimmunoglobinemia D with recurrent fever",
      "hyperimmunoglobulinemia D syndrome",
      "partial mevalonate kinase deficiency",
      "hyper IgD syndrome",
      "hyperimmunoglobulinemia D and periodic fever syndrome",
      "periodic fever Dutch type",
      "periodic fever, Dutch type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "Hyperimmunoglobinemia D with periodic fever (HIDS) is a rare autoinflammatory disease characterized by periodic attacks of fever and a systemic inflammatory reaction (cervical lymphadenopathy, abdominal pain, vomiting, diarrhea, arthralgias and skin signs)."
  },
  "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": 17945,
      "label": "mevalonate kinase deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16607,
        18150,
        19104
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021315",
          "MEDGEN:87453",
          "MESH:D054078",
          "MedDRA:10072221",
          "NANDO:2200436",
          "NORD:1260",
          "Orphanet:309025",
          "UMLS:C0342731",
          "icd11.foundation:772056052"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0017708"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6778,
      "label": "immune system disorder"
    },
    {
      "id": 17945,
      "label": "mevalonate kinase deficiency"
    }
  ]
}