{
  "id": 13568,
  "label": "insulin-resistance syndrome type A",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012520",
  "properties": {
    "xrefs": [
      "GARD:0003008",
      "MEDGEN:501111",
      "MESH:C562710",
      "NCIT:C131836",
      "OMIM:610549",
      "Orphanet:2297",
      "UMLS:C0342278",
      "icd11.foundation:343459534"
    ],
    "synonyms": [
      "insulin resistant diabetes mellitus with acanthosis nigricans and hyperandrogenism",
      "type A insulin resistance syndrome",
      "Iran, type a",
      "diabetes mellitus, insulin-resistant, with acanthosis nigricans",
      "diabetes mellitus, insulin-resistant, with acanthosis nigricans, type a",
      "insulin receptor, defect in, with insulin-resistant diabetes mellitus and acanthosis nigricans",
      "insulin-resistant acanthosis nigricans, type A"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Type A insulin-resistance syndrome belongs to the group of extreme insulin-resistance syndromes (which includes leprechaunism, the lipodystrophies, Rabson-Mendenhall syndrome and type B insulin resistance syndrome) and is characterized by the triad of hyperinsulinemia, acanthosis nigricans (skin lesions associated with insulin resistance), and signs of hyperandrogenism in females without lipodystrophy and who are not overweight."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4104,
      "label": "endocrine pancreas disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4455
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1428",
          "ICD9:251",
          "MEDGEN:124407",
          "NCIT:C27067",
          "SCTID:17346000",
          "UMLS:C0271633"
        ],
        "synonyms": [
          "disease of endocrine pancreas",
          "disease or disorder of endocrine pancreas",
          "disorder of endocrine pancreas",
          "endocrine pancreas disease",
          "endocrine pancreas disease or disorder",
          "endocrine pancreas disorder",
          "disorder of islets of langerhans",
          "disorder of pancreatic islets"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A disease involving the endocrine pancreas."
      },
      "child_count": 12,
      "reference_id": "MONDO:0001933"
    },
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4104,
      "label": "endocrine pancreas disorder"
    },
    {
      "id": 5714,
      "label": "hereditary disease"
    }
  ]
}