{
  "id": 18882,
  "label": "congenital primary megaureter",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018960",
  "properties": {
    "xrefs": [
      "GARD:0018700",
      "MEDGEN:903364",
      "NANDO:2200184",
      "Orphanet:617",
      "SCTID:717459000",
      "UMLS:C4273898",
      "icd11.foundation:566805920"
    ],
    "synonyms": [
      "congenital primary megalo-ureter",
      "CGM",
      "congenital giant megaureter",
      "congenital megalo-ureter"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ],
    "definition": "An idiopathic condition in which the bladder and bladder outlet are normal but the ureter is dilated to some extent. It may be obstructed, refluxing or unobstructed and not refluxing."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "parents": [
    {
      "id": 6948,
      "label": "kidney disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4253
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:557",
          "EFO:0003086",
          "ICD9:583.81",
          "MEDGEN:9635",
          "MESH:D007674",
          "NCIT:C3149",
          "SCTID:90708001",
          "UMLS:C0022658"
        ],
        "synonyms": [
          "disease of kidney",
          "disease or disorder of kidney",
          "disorder of kidney",
          "kidney disease",
          "kidney disease or disorder",
          "kidney disorder",
          "renal disease",
          "renal disorder",
          "nephropathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A disease involving the kidney."
      },
      "child_count": 57,
      "reference_id": "MONDO:0005240"
    },
    {
      "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": 17044,
      "label": "primary megaureter, adult-onset form",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18882
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020639",
          "MEDGEN:1842492",
          "Orphanet:238642",
          "UMLS:C5680937"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0016549"
    },
    {
      "id": 17045,
      "label": "congenital primary megaureter, obstructed form",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18882
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020640",
          "MEDGEN:1842695",
          "Orphanet:238646",
          "UMLS:C5680936",
          "icd11.foundation:342813504"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0016550"
    },
    {
      "id": 17046,
      "label": "congenital primary megaureter, refluxing form",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18882
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020641",
          "MEDGEN:1842549",
          "Orphanet:238650",
          "UMLS:C5680935",
          "icd11.foundation:1229028805"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0016551"
    },
    {
      "id": 17047,
      "label": "congenital primary megaureter, nonrefluxing and unobstructed form",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18882
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020642",
          "MEDGEN:1843330",
          "Orphanet:238654",
          "UMLS:C5680934",
          "icd11.foundation:1090144962"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0016552"
    },
    {
      "id": 22818,
      "label": "congenital primary megaureter, refluxing and obstructed form",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18882
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022236",
          "ICD10CM:Q62.2",
          "MEDGEN:1843335",
          "Orphanet:544578",
          "UMLS:C5681326"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0035295"
    }
  ],
  "roots": [
    {
      "id": 6948,
      "label": "kidney disorder"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis"
    }
  ]
}