{
  "id": 8843,
  "label": "maturity-onset diabetes of the young type 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007453",
  "properties": {
    "xrefs": [
      "DOID:0111100",
      "GARD:0010657",
      "MEDGEN:87434",
      "NANDO:2201070",
      "NCIT:C129741",
      "OMIM:125851",
      "SCTID:237604008",
      "UMLS:C0342277"
    ],
    "synonyms": [
      "GCK maturity-onset diabetes of the young (disease)",
      "GCK-associated diabetes mellitus",
      "MODY 2 monogenic diabetes type 2",
      "MODY, type II",
      "MODY2",
      "glucokinase-associated diabetes mellitus",
      "maturity onset diabetes of the Young, type 2",
      "maturity-onset diabetes of the young (disease) caused by mutation in GCK",
      "MODY, glucokinase-related",
      "MODY, type 2",
      "diabetes mellitus MODY type 2",
      "maturity-onset diabetes of the young, type 2",
      "type 2 maturity-onset diabetes of the young"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Monogenic diabetes caused by inactivating mutation(s) in the GCK gene, encoding glucokinase. Heterozygous GCK mutations may manifest as mild hyperglycemia, which is not progressive, and usually requires no treatment. Homozygous GCK mutations result in permanent neonatal diabetes."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18838,
      "label": "maturity-onset diabetes of the young",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16627,
        17928
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050524",
          "GARD:0003697",
          "HP:0004904",
          "MEDGEN:87433",
          "MESH:C562772",
          "NANDO:2200462",
          "NCIT:C114769",
          "OMIM:606391",
          "OMIMPS:125850",
          "Orphanet:552",
          "SCTID:609561005",
          "UMLS:C0342276"
        ],
        "synonyms": [
          "MODY",
          "maturity onset diabetes of the young",
          "maturity-onset diabetes of the young",
          "maturity-onset diabetes of the young (disease)",
          "Mason type diabetes"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "MODY (maturity-onset diabetes of the young) is a rare, familial, clinically and genetically heterogeneous form of diabetes characterized by young age of onset (generally 10-45 years of age) with maintenance of endogenous insulin production, lack of pancreatic beta-cell autoimmunity, absence of obesity and insulin resistance and extra-pancreatic manifestations in some subtypes."
      },
      "child_count": 30,
      "reference_id": "MONDO:0018911"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18838,
      "label": "maturity-onset diabetes of the young"
    }
  ]
}