{
  "id": 12818,
  "label": "glucose-galactose malabsorption",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011731",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 6756,
      "label": "intestinal disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6151
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5295",
          "EFO:0009431",
          "ICD9:520-579",
          "ICD9:560-569",
          "ICD9:564",
          "ICD9:564.4",
          "ICD9:569",
          "ICD9:569.4",
          "ICD9:569.49",
          "ICD9:569.89",
          "ICD9:569.9",
          "ICD9:570-579",
          "ICD9:575",
          "MEDGEN:7130",
          "MESH:D007410",
          "NCIT:C26801",
          "SCTID:85919009",
          "UMLS:C0021831"
        ],
        "synonyms": [
          "disease of intestine",
          "disease or disorder of intestine",
          "disorder of intestine",
          "intestinal disease",
          "intestinal disorder",
          "intestine disease",
          "intestine disease or disorder",
          "disease, intestinal",
          "diseases, intestinal"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          }
        ],
        "definition": "A non-neoplastic or neoplastic disorder that affects the small or large intestine."
      },
      "child_count": 58,
      "reference_id": "MONDO:0005020"
    },
    {
      "id": 19091,
      "label": "glucose transport disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17944,
        23511
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018957",
          "MEDGEN:1842427",
          "Orphanet:79178",
          "UMLS:C5389835"
        ],
        "synonyms": [
          "inborn error of glucose transport",
          "rare inborn error of glucose transport"
        ],
        "definition": "An inherited metabolic disease that is has its basis in the disruption of glucose transport."
      },
      "child_count": 6,
      "reference_id": "MONDO:0019226"
    }
  ],
  "children": [
    {
      "id": 3329,
      "label": "glucose intolerance",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4915,
        12818
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0001076"
    }
  ],
  "roots": [
    {
      "id": 6756,
      "label": "intestinal disorder"
    },
    {
      "id": 19091,
      "label": "glucose transport disorder"
    }
  ]
}