{
  "id": 21466,
  "label": "renal hypodysplasia/aplasia 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0024520",
  "properties": {
    "xrefs": [
      "GARD:0025410",
      "MEDGEN:1626497",
      "OMIM:617805",
      "UMLS:C4540497"
    ],
    "synonyms": [
      "RHDA3",
      "renal hypodysplasia/aplasia 3"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18510,
      "label": "renal agenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20383,
        23932
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:14766",
          "GARD:0009228",
          "HP:0000104",
          "HP:0008678",
          "MEDGEN:154237",
          "NANDO:2200156",
          "NCIT:C99041",
          "OMIMPS:191830",
          "Orphanet:411709",
          "SCTID:204942005",
          "UMLS:C0542519",
          "icd11.foundation:683319223"
        ],
        "synonyms": [
          "absent/small kidney",
          "absent/underdeveloped kidney",
          "renal agenesis",
          "renal agenesis (disease)",
          "renal agenesis/hypoplasia",
          "renal hypodysplasia/aplasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "Renal agenesis (RA) is a form of renal tract malformation characterized by the complete absence of development of one or both kidneys (unilateral RA or bilateral RA respectively), accompanied by absent ureter(s)."
      },
      "child_count": 12,
      "reference_id": "MONDO:0018470"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18510,
      "label": "renal agenesis"
    }
  ]
}