{
  "id": 16633,
  "label": "multicystic dysplastic kidney",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015988",
  "properties": {
    "xrefs": [
      "GARD:0018748",
      "ICD9:753.19",
      "MEDGEN:811388",
      "MESH:D021782",
      "NANDO:2200158",
      "NCIT:C123031",
      "Orphanet:1851",
      "SCTID:204962002",
      "UMLS:C3714581",
      "icd11.foundation:1178642763"
    ],
    "synonyms": [
      "MCDK",
      "multicystic renal dysplasia"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "Multicystic dysplastic kidney (MCDK) is a congenital anomaly of the kidney and urinary tract (CAKUT) in which one or both kidneys (unilateral or bilateral MCDK respectively) are large, distended by multiple cysts, and non-functional."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 4553,
      "label": "cystic kidney disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6948
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2975",
          "EFO:0008615",
          "ICD10CM:Q61",
          "ICD10WHO:Q61",
          "MEDGEN:854361",
          "MESH:D052177",
          "NANDO:2200172",
          "NCIT:C34750",
          "SCTID:722223000",
          "UMLS:C3887499"
        ],
        "synonyms": [
          "cystic renal disease",
          "kidney cyst"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A congenital or acquired kidney disorder characterized by the presence of renal cysts."
      },
      "child_count": 4,
      "reference_id": "MONDO:0002473"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29380
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD10CM:Q00-Q99",
          "MEDGEN:1843482",
          "UMLS:C0694457"
        ],
        "definition": "Any disease or disorder that disrupts the process development of an anatomical structure. Can be due to genetic or environmental causes. Typically happens during embryogenesis, but also includes post-embryonic development."
      },
      "child_count": 190,
      "reference_id": "MONDO:0021147"
    }
  ],
  "children": [
    {
      "id": 19692,
      "label": "unilateral multicystic dysplastic kidney",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16633
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019375",
          "MEDGEN:292613",
          "Orphanet:97363",
          "UMLS:C1567426"
        ],
        "synonyms": [
          "unilateral MCDK",
          "unilateral multicystic renal dysplasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "Unilateral multicystic dysplastic kidney is the form of multicystic dysplastic kidney (MCDK), a congenital anomaly of the kidney and urinary tract (CAKUT), in which one kidney is large, distended by multiple cysts, and non-functional."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019981"
    },
    {
      "id": 19693,
      "label": "bilateral multicystic dysplastic kidney",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16633
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009517",
          "MEDGEN:333563",
          "Orphanet:97364",
          "SCTID:717749002",
          "UMLS:C1840451"
        ],
        "synonyms": [
          "bilateral MCDK",
          "bilateral multicystic renal dysplasia",
          "MRD",
          "PUJO",
          "Pelvi-ureteric junction obstruction"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "Bilateral multicystic dysplastic kidney (MCDK) is a lethal form of multicystic dysplastic kidney (MCDK), a congenital anomaly of the kidney and urinary tract (CAKUT), in which both kidneys are large, distended by non-communicating multiple cysts and non-functional."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019982"
    }
  ],
  "roots": [
    {
      "id": 4553,
      "label": "cystic kidney disease"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis"
    }
  ]
}