{
  "id": 17255,
  "label": "familial visceral myopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016829",
  "properties": {
    "xrefs": [
      "GARD:0003443",
      "ICD9:359.89",
      "MEDGEN:120590",
      "OMIMPS:155310",
      "Orphanet:2604",
      "SCTID:63684002",
      "UMLS:C0266833",
      "icd11.foundation:1838806574"
    ],
    "synonyms": [
      "familial hollow visceral myopathy",
      "hereditary hollow visceral myopathy",
      "megaduodenum and/or megacystis",
      "pseudoobstruction idiopathic intestinal",
      "visceral myopathy familial"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "A rare hereditary myopathic degeneration of both gastrointestinal and urinary tracts that causes chronic intestinal pseudo-obstruction. It usually presents after the first decade of life with megaduodenum, megacystis and symptoms such as abdominal distension and/or pain, vomiting, constipation, diarrhea, dysphagia, and/or urinary tract infections.n."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 20415,
      "label": "intestinal motility disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6756
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:586448",
          "UMLS:C0400865"
        ],
        "synonyms": [
          "disorder of intestinal motility"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A disease that has its basis in the disruption of intestinal motility."
      },
      "child_count": 15,
      "reference_id": "MONDO:0021189"
    }
  ],
  "children": [
    {
      "id": 20157,
      "label": "visceral myopathy 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17255
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027875",
          "MEDGEN:1785391",
          "OMIM:155310",
          "UMLS:C5542197"
        ],
        "synonyms": [
          "visceral myopathy",
          "visceral myopathy 1",
          "VSCM",
          "infantile visceral myopathy",
          "megaduodenum and/or megacystis",
          "pseudoobstruction, idiopathic intestinal"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020754"
    },
    {
      "id": 25301,
      "label": "visceral myopathy 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17255
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016446",
          "MEDGEN:1783630",
          "OMIM:619350",
          "UMLS:C5543466"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0859157"
    }
  ],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 20415,
      "label": "intestinal motility disease"
    }
  ]
}