{
  "id": 3157,
  "label": "neuronal intestinal dysplasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000858",
  "properties": {
    "xrefs": [
      "DOID:0080072",
      "ICD9:751.5",
      "MEDGEN:576840",
      "SCTID:253783001",
      "UMLS:C0345244"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 5340,
      "label": "colonic disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        21545
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5353",
          "MEDGEN:1049",
          "MESH:D003108",
          "SCTID:128524007",
          "UMLS:C0009373"
        ],
        "synonyms": [
          "colon disease",
          "colon disease or disorder",
          "disease of colon",
          "disease or disorder of colon",
          "disorder of colon"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "Pathological processes in the colon region of the large intestine (intestine, large)."
      },
      "child_count": 13,
      "reference_id": "MONDO:0003409"
    }
  ],
  "children": [
    {
      "id": 12147,
      "label": "neuronal intestinal dysplasia, type B",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3157,
        17855
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080680",
          "GARD:0024768",
          "MEDGEN:318658",
          "OMIM:601223",
          "UMLS:C1832589"
        ],
        "synonyms": [
          "NID B",
          "neuronal intestinal dysplasia, type B"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0011021"
    },
    {
      "id": 29394,
      "label": "visceral neuropathy, familial, 1, autosomal recessive",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3157,
        17855,
        21281
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:8000011"
    }
  ],
  "roots": [
    {
      "id": 5340,
      "label": "colonic disorder"
    }
  ]
}