{
  "id": 15377,
  "label": "congenital diarrhea 7 with exudative enteropathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014375",
  "properties": {
    "xrefs": [
      "DOID:0060778",
      "GARD:0017500",
      "MEDGEN:862953",
      "OMIM:615863",
      "Orphanet:329242",
      "UMLS:C4014516"
    ],
    "synonyms": [
      "DGAT1 congenital diarrhea",
      "DGAT1 congenital diarrhoea",
      "congenital chronic diarrhea with exudative enteropathy",
      "congenital chronic diarrhea with protein-losing enteropathy",
      "congenital diarrhea caused by mutation in DGAT1",
      "congenital diarrhoea caused by mutation in DGAT1",
      "diarrhea 7, protein-losing enteropathy type",
      "diarrhea type 7",
      "diarrhoea 7, protein-losing enteropathy type",
      "diarrhoea type 7",
      "DIAR7",
      "diarrhea 7",
      "diarrhoea 7"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "Congenital chronic diarrhea with protein-losing enteropathy is a rare, genetic, intestinal disease characterized by early-onset, chronic, non-infectious, non-bloody, watery diarrhea associated with protein-losing enteropathy which results in hypoalbuminemia, hypogammaglobulinemia and elevated stool alpha-1-antitrypsin. Patients typically present severe, intractable diarrhea, failure to thrive, recurrent infections and edema."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3147,
      "label": "congenital diarrhea",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3866,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060774",
          "MEDGEN:1877146",
          "OMIMPS:214700",
          "UMLS:C6013449"
        ],
        "synonyms": [
          "diarrhea, congenital"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ]
      },
      "child_count": 24,
      "reference_id": "MONDO:0000824"
    },
    {
      "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": [],
  "roots": [
    {
      "id": 3147,
      "label": "congenital diarrhea"
    },
    {
      "id": 6756,
      "label": "intestinal disorder"
    }
  ]
}