{
  "id": 11206,
  "label": "autoimmune polyendocrinopathy type 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010012",
  "properties": {
    "xrefs": [
      "DOID:0050168",
      "GARD:0007611",
      "ICD9:258.8",
      "MEDGEN:39126",
      "NANDO:2200347",
      "NCIT:C129728",
      "NORD:824",
      "OMIM:269200",
      "Orphanet:3143",
      "SCTID:83728000",
      "UMLS:C0085860",
      "icd11.foundation:1065249344"
    ],
    "synonyms": [
      "APS type 2",
      "APS2",
      "Autoimmune Polyendocrine Syndrome Type II",
      "Schmidt syndrome",
      "autoimmune polyendocrine syndrome type 2",
      "autoimmune polyglandular syndrome type 2",
      "autoimmune thyroid disease and/or type 1 diabetes-Addison disease syndrome",
      "APS 2",
      "PGA 2",
      "Schmidt's syndrome",
      "autoimmune polyendocrine syndrome, type II",
      "diabetes mellitus, Addison disease, myxedema",
      "diabetes mellitus, Addison's disease, myxedema",
      "multiple endocrine deficiency syndrome, type 2",
      "polyendocrine autoimmune syndrome, type 2",
      "polyglandular autoimmune syndrome, type 2",
      "polyglandular deficiency syndrome type 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Autoimmune polyglandular syndrome of likely polygenic etiology characterized by the presence of primary adrenal insufficiency in association with autoimmune thyroiditis and/or type 1 diabetes mellitus; this condition is not associated with mucocutaneous candidiasis."
  },
  "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"
    }
  ]
}