{
  "id": 29394,
  "label": "visceral neuropathy, familial, 1, autosomal recessive",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:8000011",
  "properties": {
    "xrefs": [
      "DOID:0080679",
      "GARD:0003928",
      "MEDGEN:340946",
      "MESH:C537394",
      "OMIM:243180",
      "Orphanet:99811",
      "UMLS:C1855733"
    ],
    "synonyms": [
      "Argyrophil myenteric plexus deficiency of",
      "Argyrophil myenteric plexus, deficiency of",
      "NID A",
      "intestinal pseudoobstruction due to neuronal disease",
      "neuronal intestinal dysplasia, type a",
      "pseudoobstruction chronic idiopathic intestinal neuronal type",
      "pseudoobstruction, chronic idiopathic intestinal, neuronal type",
      "visceral neuropathy familial",
      "visceral neuropathy, familial, autosomal recessive"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "A form of chronic intestinal pseudoobstruction caused by a developmental failure of the enteric neurons to differentiate or migrate properly and manifests as a bowel obstruction."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3157,
      "label": "neuronal intestinal dysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5340
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080072",
          "ICD9:751.5",
          "MEDGEN:576840",
          "SCTID:253783001",
          "UMLS:C0345244"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0000858"
    },
    {
      "id": 17855,
      "label": "chronic intestinal pseudoobstruction",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4829,
        20415
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0012744",
          "MEDGEN:536759",
          "NANDO:1200458",
          "NANDO:2200946",
          "NORD:970",
          "Orphanet:2978",
          "SCTID:235828008",
          "UMLS:C0238062"
        ],
        "synonyms": [
          "CIPO",
          "Chronic Intestinal Pseudo-Obstruction",
          "chronic intestinal pseudo-obstruction",
          "cipo",
          "intestinal pseudo-obstruction, chronic"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "Chronic intestinal pseudo-obstruction (CIPO) is a rare gastrointestinal motility disorder characterized by recurring episodes resembling mechanical obstruction in the absence of organic, systemic, or metabolic disorders, and without any physical obstruction being detected by X-ray or during surgery. CIPO develops predominantly in children and may be present at birth."
      },
      "child_count": 10,
      "reference_id": "MONDO:0017574"
    },
    {
      "id": 21281,
      "label": "visceral neuropathy, familial",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:540202",
          "OMIMPS:243180",
          "UMLS:C0266834"
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0023961"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3157,
      "label": "neuronal intestinal dysplasia"
    },
    {
      "id": 17855,
      "label": "chronic intestinal pseudoobstruction"
    },
    {
      "id": 21281,
      "label": "visceral neuropathy, familial"
    }
  ]
}