Lactose Intolerance

Alias:
Lactose Malabsorption
Intolerance or Malabsorption of Lactose
Lm - [lactose Malabsorption]
Lm - Lactose Malabsorption
Milk Sugar Intolerance
Cow Milk Enteropathy
Milk Intolerance
Hypolactasia
Alactasia
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Lactose Intolerance, also known as lactose malabsorption, is related to lactose intolerance, adult type and lactase deficiency, congenital, and has symptoms including abdominal pain, constipation and diarrhea. An important gene associated with Lactose Intolerance is LCT (Lactase), and among its related pathways/superpathways are Digestion and absorption and Diseases of carbohydrate metabolism. The drugs Caseins and Sorbitol have been mentioned in the context of this disorder. Affiliated tissues include small intestine and breast, and related phenotypes are Reduced mammosphere formation and endocrine/exocrine gland
Related ID:
MESH:D007787
ICD11:1026224967

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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22
184
3

Medical Symptom

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Gene & Mutation

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MGI
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References Literature

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