{
  "id": 8807,
  "label": "Balkan nephropathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007416",
  "properties": {
    "xrefs": [
      "DOID:3052",
      "EFO:0007164",
      "GARD:0008576",
      "ICD10CM:N15.0",
      "ICD9:583.89",
      "MEDGEN:495",
      "MESH:D001449",
      "NCIT:C123025",
      "OMIM:124100",
      "SCTID:26121002",
      "UMLS:C0004698",
      "icd11.foundation:18497836"
    ],
    "synonyms": [
      "Balkan endemic nephropathy",
      "Chinese herb endemic nephropathy",
      "Danubian endemic familial nephropathy",
      "aristolochic acid nephropathy",
      "endemic nephropathy",
      "AAN",
      "BEN",
      "DEFN",
      "nephropathia epidemica"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "A chronic tubulointerstitial nephropathy that affects people in certain rural areas along the Danube river in the Balkans. It leads to end-stage renal disease."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3337,
      "label": "interstitial nephritis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3410
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1063",
          "ICD10CM:N10-N16",
          "ICD9:583.89",
          "MEDGEN:11952",
          "MESH:D009395",
          "NANDO:2200136",
          "NCIT:C26834",
          "SCTID:28689008",
          "UMLS:C0041349"
        ],
        "synonyms": [
          "Tubulointerstitial nephritis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "Inflammation of the renal tubules and supporting tissues of the kidney."
      },
      "child_count": 2,
      "reference_id": "MONDO:0001085"
    },
    {
      "id": 7021,
      "label": "hereditary nephritis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3410,
        23932
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:10305",
          "MESH:D009394",
          "SCTID:399340005",
          "UMLS:C0027706"
        ],
        "synonyms": [
          "hereditary nephritis",
          "familial nephritis",
          "nephritis, familial"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A group of inherited conditions characterized initially by hematuria and slowly progressing to renal insufficiency. The most common form is the Alport syndrome (hereditary nephritis with hearing loss) which is caused by mutations in genes for type IV collagen and defective glomerular basement membrane."
      },
      "child_count": 14,
      "reference_id": "MONDO:0005334"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3337,
      "label": "interstitial nephritis"
    },
    {
      "id": 7021,
      "label": "hereditary nephritis"
    }
  ]
}