{
  "id": 15458,
  "label": "Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014458",
  "properties": {
    "xrefs": [
      "DOID:0080760",
      "GARD:0016048",
      "MEDGEN:863399",
      "OMIM:616026",
      "UMLS:C4014962"
    ],
    "synonyms": [
      "Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young",
      "Fanconi syndrome caused by mutation in HNF4A",
      "HNF4A Fanconi syndrome",
      "fanconi renotubular syndrome 4, with maturity-onset diabetes of the young",
      "FRTS4",
      "FRTS4 with MODY"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Any Fanconi syndrome in which the cause of the disease is a mutation in the HNF4A gene."
  },
  "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"
    },
    {
      "id": 23978,
      "label": "inherited Fanconi renotubular syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3335,
        16626
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026093",
          "OMIMPS:134600"
        ],
        "synonyms": [
          "hereditary Fanconi renotubular syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "An instance of Fanconi renotubular syndrome that is inherited."
      },
      "child_count": 6,
      "reference_id": "MONDO:0100238"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18838,
      "label": "maturity-onset diabetes of the young"
    },
    {
      "id": 23978,
      "label": "inherited Fanconi renotubular syndrome"
    }
  ]
}