{
  "id": 14910,
  "label": "karyomegalic interstitial nephritis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013898",
  "properties": {
    "xrefs": [
      "DOID:0060911",
      "GARD:0011003",
      "MEDGEN:766688",
      "NCIT:C173626",
      "OMIM:614817",
      "Orphanet:401996",
      "UMLS:C3553774"
    ],
    "synonyms": [
      "FAN1 interstitial nephritis",
      "KIN",
      "KMIN",
      "interstitial nephritis caused by mutation in FAN1",
      "karyomegalic interstitial nephritis",
      "kin",
      "systemic karyomegaly",
      "interstitial nephritis, karyomegalic"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "Any interstitial nephritis in which the cause of the disease is a mutation in the FAN1 gene."
  },
  "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"
    },
    {
      "id": 20416,
      "label": "DNA repair disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18954
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0008499",
          "GARD:0025299",
          "MEDGEN:82774",
          "MESH:D049914",
          "NCIT:C7757",
          "UMLS:C0268134"
        ],
        "synonyms": [
          "DNA repair disorder",
          "deficiency of DNA repair",
          "disorder of DNA repair",
          "DNA Repairs, deficient",
          "DNA repair deficiency",
          "DNA repair deficiency disorders",
          "DNA repair, deficient",
          "DNA repair-deficiencies",
          "DNA repair-deficiency",
          "DNA repair-deficiency disorder",
          "Repairs, deficient DNA",
          "chromosome instability syndrome",
          "chromosome instability syndromes",
          "deficient DNA Repairs",
          "deficient DNA repair",
          "disorder, DNA repair-deficiency",
          "disorders, DNA repair-deficiency",
          "repair, deficient DNA",
          "syndrome, chromosome instability",
          "syndromes, chromosome instability"
        ],
        "definition": "A disease that has its basis in the disruption of DNA repair."
      },
      "child_count": 16,
      "reference_id": "MONDO:0021190"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3337,
      "label": "interstitial nephritis"
    },
    {
      "id": 7021,
      "label": "hereditary nephritis"
    },
    {
      "id": 20416,
      "label": "DNA repair disease"
    }
  ]
}