{
  "id": 21197,
  "label": "global disaccharide intolerance",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0023250",
  "properties": {
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10361,
      "label": "congenital sucrase-isomaltase deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6659,
        17944
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111633",
          "GARD:0006183",
          "ICD9:271.3",
          "MEDGEN:220924",
          "MESH:C538139",
          "MedDRA:10066387",
          "NANDO:2200908",
          "NCIT:C128190",
          "NORD:1056",
          "OMIM:222900",
          "Orphanet:35122",
          "SCTID:78373000",
          "UMLS:C1283620",
          "icd11.foundation:1817406536"
        ],
        "synonyms": [
          "CSID",
          "congenital sucrase-isomaltase deficiency",
          "congenital sucrose intolerance",
          "disaccharide intolerance",
          "genetic sucrase-isomaltose malabsorption",
          "sucrase-isomaltase deficiency",
          "SI deficiency",
          "congenital sucrose malabsorption",
          "congenital sucrose-isomaltase intolerance",
          "congenital sucrose-isomaltase malabsorption",
          "disaccharide intolerance 1",
          "disaccharide intolerance i",
          "disaccharide intolerance, 1",
          "intestinal sucrase-a-dextrinase deficiency",
          "invertase deficiency",
          "sucrase-alpha-dextrinase deficiency",
          "sucrase-isomaltase deficiency, congenital",
          "sucrose intolerance congenital",
          "sucrose intolerance, congenital",
          "sucrose isomaltose enzyme deficiency",
          "sucrose-isomaltase malabsorption, congenital",
          "sucrose-isomaltose malabsorption, congenital"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A disorder of carbohydrate absorption and transport caused by autosomal recessive mutation of the SI gene, characterized by malabsorption of sucrose and maltose."
      },
      "child_count": 12,
      "reference_id": "MONDO:0009114"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10361,
      "label": "congenital sucrase-isomaltase deficiency"
    }
  ]
}