{
  "id": 9249,
  "label": "primary intestinal lymphangiectasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007916",
  "properties": {
    "xrefs": [
      "GARD:0007873",
      "ICD9:457.1",
      "MEDGEN:444009",
      "NORD:1609",
      "OMIM:152800",
      "Orphanet:90362",
      "SCTID:6124009",
      "UMLS:C2931241",
      "icd11.foundation:52162548"
    ],
    "synonyms": [
      "Waldmann disease",
      "Waldmann's disease",
      "familial Waldmann's disease (type)",
      "lymphangiectasia, intestinal",
      "primary intestinal lymphangiectasis"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "Primary intestinal lymphangiectasia (PIL) is a rare intestinal disease characterized by dilated intestinal lacteals which cause lymph leakage into the small bowel lumen. Clinical manifestations include edema related to hypoalbuminemia (protein-losing enteropathy), asthenia, diarrhea, lymphedema and failure to thrive in children."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18321,
      "label": "intestinal lymphangiectasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6756
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0012331",
          "HP:0002593",
          "ICD9:457.1",
          "MEDGEN:9828",
          "MedDRA:10025213",
          "NANDO:2100256",
          "NANDO:2200914",
          "Orphanet:36204",
          "SCTID:197260007",
          "UMLS:C0024215",
          "icd11.foundation:1255239964"
        ],
        "synonyms": [
          "intestinal lymphangiectasia",
          "intestinal lymphangiectasia (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "Dilatation of the intestinal lymphatic system usually caused by an obstruction in the intestinal wall. It may be congenital or acquired and is characterized by diarrhea; hypoproteinemia; peripheral and/or abdominal edema; and protein-losing enteropathies."
      },
      "child_count": 2,
      "reference_id": "MONDO:0018178"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18321,
      "label": "intestinal lymphangiectasia"
    }
  ]
}