{
  "id": 3329,
  "label": "glucose intolerance",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001076",
  "properties": {
    "xrefs": [
      "DOID:10603",
      "ICD9:271.3",
      "MEDGEN:75760",
      "MESH:D018149",
      "NCIT:C34646",
      "SCTID:267426009",
      "UMLS:C0271650",
      "icd11.foundation:1392580302"
    ],
    "synonyms": [
      "glucose: [intolerance] or [malabsorption]",
      "glucose: intolerance",
      "glucose: malabsorption"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      }
    ],
    "definition": "The inability to regulate blood glucose levels resulting in hyperglycemia."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4915,
      "label": "glucose metabolism disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6795
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4194",
          "EFO:0009406",
          "ICD9:271.8",
          "MEDGEN:226229",
          "MESH:D044882",
          "NCIT:C53655",
          "SCTID:126877002",
          "UMLS:C1257958"
        ],
        "synonyms": [
          "disorder of glucose metabolism",
          "glucose metabolism disorder"
        ],
        "definition": "A metabolic disorder characterized by abnormal blood glucose levels."
      },
      "child_count": 9,
      "reference_id": "MONDO:0002908"
    },
    {
      "id": 12818,
      "label": "glucose-galactose malabsorption",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6756,
        19091
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070563",
          "GARD:0006521",
          "ICD9:271.3",
          "MEDGEN:78647",
          "MESH:C562602",
          "MedDRA:10066388",
          "NANDO:2200909",
          "NORD:1190",
          "OMIM:606824",
          "Orphanet:35710",
          "SCTID:190749000",
          "UMLS:C0268186",
          "icd11.foundation:2108415931"
        ],
        "synonyms": [
          "SGLT1 deficiency",
          "glucose-galactose malabsorption",
          "Complex carbohydrate intolerance",
          "GGM",
          "carbohydrate intolerance of glucose galactose",
          "glucose galactose malabsorption deficiency",
          "glucose/galactose malabsorption",
          "monosaccharide malabsorption"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "Glucose-galactose malabsorption (GGM) is a very rare, potentially lethal, genetic metabolic disease characterized by impaired glucose-galactose absorption resulting in severe watery diarrhea and dehydration with onset inthe neonatal period."
      },
      "child_count": 2,
      "reference_id": "MONDO:0011731"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4915,
      "label": "glucose metabolism disease"
    },
    {
      "id": 12818,
      "label": "glucose-galactose malabsorption"
    }
  ]
}