{
  "id": 23281,
  "label": "collagenous sprue",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0044092",
  "properties": {
    "xrefs": [
      "MEDGEN:137953",
      "MESH:D064068",
      "NCIT:C45426",
      "SCTID:61738006",
      "UMLS:C0341299",
      "icd11.foundation:562877246"
    ],
    "synonyms": [
      "collagenous sprue",
      "non-gluten sensitive enteropathy syndrome",
      "Sprues, collagenous",
      "collagenous Sprues",
      "collagenous enteropathy",
      "collagenous enteropathy syndrome",
      "non-gluten intolerance syndrome",
      "sprue, collagenous"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "A rare disorder affecting the digestive tract. Its cause is unclear but may be attributed, in part, to increased collagen synthesis without adequate fibrolysis. It is characterized histologically by atrophy of mucosal villi and crypts with extensive subepithelial collagen deposition. Clinical signs include nausea, vomiting, diarrhea and weight loss. Unlike celiac sprue (celiac disease), a gluten-free diet does not predict a certain regression of the disease. The clinical course follows a progression of malabsorption leading to nutritional deficiencies, small bowel ulceration/perforation, lymphoma and infection. Prognosis is usually dismal."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "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"
    },
    {
      "id": 6795,
      "label": "metabolic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29380
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0014667",
          "EFO:0000589",
          "ICD10CM:E70-E88",
          "ICD10WHO:E70-E90",
          "ICD9:277.8",
          "ICD9:277.9",
          "MEDGEN:44376",
          "MESH:D008659",
          "NANDO:1100002",
          "NCIT:C3235",
          "SCTID:75934005",
          "UMLS:C0025517"
        ],
        "synonyms": [
          "disorder of metabolic process",
          "metabolic disease",
          "metabolic disorder",
          "metabolic process disease",
          "disease of metabolism"
        ],
        "definition": "A congenital disorder (due to inherited enzyme abnormality) or acquired (due to failure of a metabolically important organ) disorder resulting from an abnormal metabolic process."
      },
      "child_count": 37,
      "reference_id": "MONDO:0005066"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6756,
      "label": "intestinal disorder"
    },
    {
      "id": 6795,
      "label": "metabolic disease"
    }
  ]
}