{
  "id": 12758,
  "label": "maturity-onset diabetes of the young type 6",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011668",
  "properties": {
    "xrefs": [
      "DOID:0111104",
      "GARD:0010660",
      "MEDGEN:344030",
      "MESH:C565231",
      "NCIT:C129745",
      "OMIM:606394",
      "SCTID:609573005",
      "UMLS:C1853371"
    ],
    "synonyms": [
      "MODY6",
      "NEUROD1 maturity-onset diabetes of the young (disease)",
      "NEUROD1-associated monogenic diabetes",
      "maturity onset diabetes of the Young, type 6",
      "maturity-onset diabetes of the young (disease) caused by mutation in NEUROD1",
      "maturity-onset diabetes of the young 6",
      "neurogenic differentiation Factor 1-associated monogenic diabetes",
      "MODY NEUROD1 related",
      "MODY, type 6",
      "diabetes mellitus MODY type 6",
      "maturity-onset diabetes of the young, type 6",
      "type 6 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 gene NEUROD1, encoding neurogenic differentiation 1. In addition to diabetes, this condition may be associated with neurogenic anomalies. Homozygous NEUROD1 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"
    }
  ]
}