{
  "id": 20893,
  "label": "bilateral renal agenesis dominant type",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0022572",
  "properties": {
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16631,
      "label": "bilateral renal agenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18510
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080200",
          "GARD:0016579",
          "ICD10CM:Q60.1",
          "MEDGEN:296299",
          "NCIT:C101219",
          "NORD:1656",
          "Orphanet:1848",
          "UMLS:C1609433"
        ],
        "synonyms": [
          "Renal Agenesis, Bilateral",
          "bilateral renal aplasia",
          "renal agenesis, bilateral"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "Bilateral renal agenesis is the most profound form of renal agenesis, characterized by complete absence of kidney development, absent ureters and subsequent absence of fetal renal function resulting in Potter sequence with pulmonary hypoplasia related to oligohydramnios, which is fatal shortly after birth."
      },
      "child_count": 1,
      "reference_id": "MONDO:0015986"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16631,
      "label": "bilateral renal agenesis"
    }
  ]
}