{
  "id": 18321,
  "label": "intestinal lymphangiectasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018178",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 6756,
      "label": "intestinal disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6151
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5295",
          "EFO:0009431",
          "ICD9:520-579",
          "ICD9:560-569",
          "ICD9:564",
          "ICD9:564.4",
          "ICD9:569",
          "ICD9:569.4",
          "ICD9:569.49",
          "ICD9:569.89",
          "ICD9:569.9",
          "ICD9:570-579",
          "ICD9:575",
          "MEDGEN:7130",
          "MESH:D007410",
          "NCIT:C26801",
          "SCTID:85919009",
          "UMLS:C0021831"
        ],
        "synonyms": [
          "disease of intestine",
          "disease or disorder of intestine",
          "disorder of intestine",
          "intestinal disease",
          "intestinal disorder",
          "intestine disease",
          "intestine disease or disorder",
          "disease, intestinal",
          "diseases, intestinal"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A non-neoplastic or neoplastic disorder that affects the small or large intestine."
      },
      "child_count": 58,
      "reference_id": "MONDO:0005020"
    }
  ],
  "children": [
    {
      "id": 9249,
      "label": "primary intestinal lymphangiectasia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18321
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007916"
    },
    {
      "id": 19379,
      "label": "secondary intestinal lymphangiectasia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18321
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019135",
          "MEDGEN:908114",
          "Orphanet:90363",
          "SCTID:717255008",
          "UMLS:C4273969",
          "icd11.foundation:1730894033"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "Secondary intestinal lymphangiectasia is an acquired from of intestinal lymphangiectasia manifesting as a protein-losing enteropathy due to another disorder such as CrohnBs disease, congestive heart failure, sarcoidosis, Turner syndrome and often in patients who have undergone a Fontan operation. It is characterized by malabsorption, diarrhea, edema due hypoproteinemia, steatorrhea and serosal effusions."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019574"
    }
  ],
  "roots": [
    {
      "id": 6756,
      "label": "intestinal disorder"
    }
  ]
}