{
    "disease_id": "DOID:0070563",
    "recommended_name": {
        "id": "DOID:0070563",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070563",
        "name": "glucose-galactose malabsorption",
        "description": "A glucose metabolism disease characterized by a defect in glucose and galactose transport across the intestinal brush border, resulting in neonatal onset of life-threatening watery diarrhea and dehydration, that has_material_basis_in homozygous mutation in the SLC5A1 gene on chromosome 22q12.3."
    },
    "synonyms": [
        {
            "id": "DOID:0070563",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070563",
            "name": "GGM",
            "description": ""
        },
        {
            "id": "DOID:0070563",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070563",
            "name": "SGLT1 deficiency",
            "description": ""
        },
        {
            "id": "DOID:0070563",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070563",
            "name": "monosaccharide malabsorption",
            "description": ""
        },
        {
            "id": "MONDO:0011731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011731",
            "name": "glucose-galactose malabsorption",
            "description": "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."
        },
        {
            "id": "MONDO:0011731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011731",
            "name": "SGLT1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011731",
            "name": "glucose-galactose malabsorption",
            "description": ""
        },
        {
            "id": "MONDO:0011731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011731",
            "name": "Complex carbohydrate intolerance",
            "description": ""
        },
        {
            "id": "MONDO:0011731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011731",
            "name": "GGM",
            "description": ""
        },
        {
            "id": "MONDO:0011731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011731",
            "name": "carbohydrate intolerance of glucose galactose",
            "description": ""
        },
        {
            "id": "MONDO:0011731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011731",
            "name": "glucose galactose malabsorption deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011731",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011731",
            "name": "glucose/galactose malabsorption",
            "description": ""
        },
        {
            "id": "MIM:606824",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/606824",
            "name": "Congenital glucose/galactose malabsorption",
            "description": "Congenital glucose/galactose malabsorption"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070563"
    ],
    "unlinked_id_list": []
}