{
  "id": 10941,
  "label": "nephronophthisis 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009728",
  "properties": {
    "xrefs": [
      "DOID:0111112",
      "GARD:0018645",
      "MEDGEN:343406",
      "MESH:C537699",
      "NANDO:1201036",
      "NANDO:2200140",
      "NCIT:C74998",
      "OMIM:256100",
      "Orphanet:93592",
      "SCTID:444830001",
      "UMLS:C1855681"
    ],
    "synonyms": [
      "NPH1",
      "NPHP1",
      "NPHP1 nephronophthisis (disease)",
      "familial juvenile nephronophthisis",
      "juvenile nephronophthisis",
      "nephronophthisis (disease) caused by mutation in NPHP1",
      "nephronophthisis 1",
      "nephronophthisis 1, juvenile",
      "nephronophthisis type 1",
      "Nph1",
      "nephronophthisis, familial juvenile"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Progressive tubulointerstitial nephritis inherited in an autosomal recessive manner. It is caused by mutations in the NPHP1 gene. Patients present with anemia, polyuria, and polydipsia during childhood. The progressive bilateral kidney damage results in renal failure."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 7000,
      "label": "ciliopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        29384
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060340",
          "EFO:0003900",
          "GARD:0021544",
          "GTR:AN0966173",
          "MEDGEN:908923",
          "Orphanet:363250",
          "UMLS:C4277690"
        ],
        "synonyms": [
          "ciliopathy",
          "ciliopathies"
        ],
        "definition": "A genetic disorder of the cellular cilia or the cilia anchoring structures, the basal bodies, or of ciliary function."
      },
      "child_count": 72,
      "reference_id": "MONDO:0005308"
    },
    {
      "id": 18920,
      "label": "nephronophthisis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7611,
        16626
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12712",
          "GARD:0000206",
          "HP:0000090",
          "MEDGEN:146912",
          "NANDO:1201036",
          "NANDO:2100015",
          "NANDO:2200140",
          "NANDO:2200170",
          "NCIT:C123200",
          "OMIMPS:256100",
          "Orphanet:655",
          "UMLS:C0687120",
          "icd11.foundation:158151813"
        ],
        "synonyms": [
          "medullary cystic kidney",
          "nephronophthisis",
          "nephronophthisis (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "Progressive tubulointerstitial injury, inherited in an autosomal recessive pattern, caused by mutations in genes involved in ciliary function, which may result in an end stage renal failure."
      },
      "child_count": 36,
      "reference_id": "MONDO:0019005"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 7000,
      "label": "ciliopathy"
    },
    {
      "id": 18920,
      "label": "nephronophthisis"
    }
  ]
}