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ENLactase Deficiency, Congenital (COLACD)
Alias:
Congenital Lactase Deficiency
Disaccharide Intolerance Ii
Congenital Lactose Malabsorption
Congenital Lactose Intolerance
Congenital Alactasia Syndrome
Congenital Alactasia
Hereditary Alactasia
Cld - [congenital Lactase Deficiency]
Disaccharide Intolerance Type 2
Lactose Intolerance of Newborn
Hereditary Lactase Deficiency
Disaccharide Intolerance 2
Alactasia, Congenital
Colacd
Cld
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Lactase Deficiency, Congenital, also known as congenital lactase deficiency, is related to lactose intolerance and lactose intolerance, adult type. An important gene associated with Lactase Deficiency, Congenital is LCT (Lactase), and among its related pathways/superpathways are Disorders of transmembrane transporters and HIF1Alpha Pathway. Affiliated tissues include breast and thyroid, and related phenotypes are dehydration and metabolic acidosis
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MALACARDS
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