{
  "id": 8451,
  "label": "prune belly syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007032",
  "properties": {
    "xrefs": [
      "DOID:0060889",
      "GARD:0007479",
      "ICD10CM:Q79.4",
      "ICD9:756.71",
      "MEDGEN:18718",
      "MESH:D011535",
      "MedDRA:10051025",
      "NANDO:2200185",
      "NCIT:C85033",
      "NORD:1623",
      "OMIM:100100",
      "Orphanet:2970",
      "SCTID:5187006",
      "UMLS:C0033770",
      "icd11.foundation:1393408621"
    ],
    "synonyms": [
      "Obrinsky syndrome",
      "Obrisnksy syndrome",
      "abdominal muscle deficiency syndrome",
      "eagle-Barret syndrome",
      "prune belly syndrome",
      "syndrome of agenesis of abdominal muscles",
      "triad syndrome",
      "PBS",
      "abdominal muscles, absence of, with urinary tract Abnormality and cryptorchidism",
      "eagle-Barrett syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Prune belly syndrome is a rare congenital disorder, belonging to the group of fetal lower urinary tract obstructions (LUTO), involving variable dilation of the lower urinary tract in association with partial or complete absence of the lateral and inferior abdominal wall musculature and in males bilateral non-palpable undescended testes."
  },
  "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": 18571,
      "label": "fetal lower urinary tract obstruction",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6948,
        19192
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021804",
          "MEDGEN:931214",
          "Orphanet:435365",
          "SCTID:717752005",
          "UMLS:C4305545",
          "icd11.foundation:1661120971"
        ],
        "synonyms": [
          "LUTO"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 10,
      "reference_id": "MONDO:0018559"
    },
    {
      "id": 23932,
      "label": "inherited kidney disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6948
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "genetic renal disease",
          "inherited kidney disease",
          "inherited renal disorder",
          "nephrogenetic disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions, with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that are characterized by abnormalities in the kidney or urinary system."
      },
      "child_count": 52,
      "reference_id": "MONDO:0100191"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 18571,
      "label": "fetal lower urinary tract obstruction"
    },
    {
      "id": 23932,
      "label": "inherited kidney disorder"
    }
  ]
}