{
  "id": 16938,
  "label": "autoimmune polyendocrinopathy type 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016422",
  "properties": {
    "xrefs": [
      "GARD:0010980",
      "ICD9:258.1",
      "MEDGEN:453060",
      "Orphanet:227982",
      "SCTID:449731009",
      "UMLS:C1535942",
      "icd11.foundation:1361747293"
    ],
    "synonyms": [
      "APS type 3",
      "APS3",
      "autoimmune polyendocrine syndrome type 3",
      "autoimmune polyglandular syndrome type 3",
      "PAS3",
      "polyglandular autoimmune syndrome type 3"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "A rare, endocrine disease characterized by autoimmune thyroid disease associated with at least one other autoimmune disease, such as type I diabetes mellitus, chronic atrophic gastritis, pernicious anemia, vitiligo, alopecia, or myasthenia gravis, but excluding Addison disease."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17602,
      "label": "autoimmune polyendocrinopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2997,
        4370,
        16071
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:14040",
          "GARD:0021116",
          "ICD10CM:E31.0",
          "ICD9:258.8",
          "MEDGEN:39042",
          "NANDO:2100125",
          "NCIT:C129726",
          "NCIT:C84576",
          "NORD:790",
          "Orphanet:282196",
          "SCTID:41864002",
          "UMLS:C0085409",
          "icd11.foundation:548357900"
        ],
        "synonyms": [
          "APS",
          "Antiphospholipid Syndrome",
          "autoimmune polyendocrine syndrome",
          "autoimmune polyendocrine syndrome; polyglandular autoimmune syndrome",
          "autoimmune polyendocrinopathy",
          "autoimmune polyendocrinopathy syndrome",
          "autoimmune polyglandular failure",
          "autoimmune polyglandular syndrome",
          "autoimmune polyglandular syndrome(s)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A group of diverse conditions that are characterized by spontaneous, multi-organ autoimmunity, which target both endocrine (adrenal, gonad, pancreatic islet cells, parathyroid, pituitary, thyroid) and non-endocrine (gastrointestinal, integumentary, lymphatic) tissues."
      },
      "child_count": 12,
      "reference_id": "MONDO:0017278"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17602,
      "label": "autoimmune polyendocrinopathy"
    }
  ]
}