{
    "disease_id": "DOID:0111646", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009115", 
            "name": "Alactasia, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009115", 
            "name": "lactase deficiency, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009115", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009115", 
            "name": "disaccharide intolerance 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111646", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111646", 
            "name": "CLD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111646", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111646", 
            "name": "congenital alactasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111646", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111646", 
            "name": "congenital alactasia syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111646", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111646", 
            "name": "congenital lactose intolerance"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111646", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111646", 
            "name": "congenital lactose malabsorption"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111646", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111646", 
            "name": "disaccharide intolerance II"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111646", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111646", 
        "name": "congenital lactase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/223000", 
            "id": "223000", 
            "database": "MIM"
        }
    ]
}