{
  "id": 10854,
  "label": "microvillus inclusion disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009635",
  "properties": {
    "xrefs": [
      "DOID:0060775",
      "GARD:0007039",
      "ICD9:579.8",
      "MEDGEN:137954",
      "MedDRA:10068494",
      "NANDO:2100255",
      "NANDO:2200913",
      "NORD:1446",
      "OMIM:251850",
      "Orphanet:2290",
      "SCTID:235729009",
      "UMLS:C0341306",
      "icd11.foundation:2137578537"
    ],
    "synonyms": [
      "Davidson disease",
      "MVID",
      "MYO5B secretory diarrhea",
      "MYO5B secretory diarrhoea",
      "congenital familial protracted diarrhea with enterocyte brush-border abnormalities",
      "congenital familial protracted diarrhoea with enterocyte brush-border abnormalities",
      "congenital microvillous atrophy",
      "congenital microvillus atrophy",
      "diarrhoea 2 with microvillus atrophy",
      "microvillous inclusion disease",
      "microvillus inclusion disease",
      "secretory diarrhea caused by mutation in MYO5B",
      "secretory diarrhoea caused by mutation in MYO5B",
      "DIAR2",
      "Davidson's disease",
      "congenital familial protracted diarrhea",
      "congenital familial protracted diarrhea with enterocyte Brush-border abnormalities",
      "congenital familial protracted diarrhoea",
      "congenital familial protracted diarrhoea with enterocyte Brush-border abnormalities",
      "diarrhea 2, with microvillus atrophy",
      "diarrhoea 2, with microvillus atrophy",
      "familial enteropathy, microvillus",
      "intractable diarrhea of infancy",
      "intractable diarrhoea of infancy",
      "microvillus atrophy, congenital"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "Microvillus inclusion disease (MVID) is a very rare, severe, malabsorbative syndrome characterized clinically by protracted or intractable neonatal secretory diarrhea and histologically by inclusion bodies on the intestinal epithelium."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 23521,
      "label": "congenital secretory diarrhea",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2794,
        3147
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD9:579.8",
          "MEDGEN:82757",
          "SCTID:25898005",
          "UMLS:C0267661"
        ],
        "synonyms": [
          "congenital secretory diarrhea"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ]
      },
      "child_count": 10,
      "reference_id": "MONDO:0045032"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 23521,
      "label": "congenital secretory diarrhea"
    }
  ]
}