{
    "disease_id": "DOID:0111646",
    "recommended_name": {
        "id": "DOID:0111646",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111646",
        "name": "congenital lactase deficiency",
        "description": "A carbohydrate metabolic disorder characterized by watery diarrhea in infants fed with breast milk or other lactose-containing formulas that has_material_basis_in homozygous or compound heterozygous mutation in LCT on chromosome 2q21.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111646",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111646",
            "name": "CLD",
            "description": ""
        },
        {
            "id": "DOID:0111646",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111646",
            "name": "congenital alactasia",
            "description": ""
        },
        {
            "id": "DOID:0111646",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111646",
            "name": "congenital alactasia syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111646",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111646",
            "name": "congenital lactose intolerance",
            "description": ""
        },
        {
            "id": "DOID:0111646",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111646",
            "name": "congenital lactose malabsorption",
            "description": ""
        },
        {
            "id": "DOID:0111646",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111646",
            "name": "disaccharide intolerance II",
            "description": ""
        },
        {
            "id": "MONDO:0009115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009115",
            "name": "congenital lactase deficiency",
            "description": "Congenital lactase deficiency is a rare severe gastrointestinal disorder in newborns primarily reported in Finland and characterized clinically by watery diarrhea on feeding with breast-milk or lactose-containing formula."
        },
        {
            "id": "MONDO:0009115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009115",
            "name": "Alactasia, congenital",
            "description": ""
        },
        {
            "id": "MONDO:0009115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009115",
            "name": "lactase deficiency, congenital",
            "description": ""
        },
        {
            "id": "MONDO:0009115",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009115",
            "name": "disaccharide intolerance 2",
            "description": ""
        },
        {
            "id": "MIM:223000",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/223000",
            "name": "Congenital lactase deficiency",
            "description": "Congenital lactase deficiency"
        }
    ]
}