Congenital lactase deficiency (Q40033): Difference between revisions
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Revision as of 05:41, 13 August 2026
This is a congenital deficiency of lactase (EC 3.2.1.108), inherited as an autosomal recessive trait, presenting in infancy and manifested by profuse watery diarrhoea in response to dietary milk, due to inability to digest lactose, a sugar found in milk and to a lesser extent milk-derived dairy products. The condition may lead to marasmus and death if lactose is not eliminated from the diet.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C61.61 |
||
| English | Congenital lactase deficiency |
This is a congenital deficiency of lactase (EC 3.2.1.108), inherited as an autosomal recessive trait, presenting in infancy and manifested by profuse watery diarrhoea in response to dietary milk, due to inability to digest lactose, a sugar found in milk and to a lesser extent milk-derived dairy products. The condition may lead to marasmus and death if lactose is not eliminated from the diet. |
Statements
CID11:5C61.61
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dki-india-5C61.61
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Concluído
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