Acquired monosaccharide malabsorption

Description

This is an acquired condition in which the cells lining the intestine cannot take in one or all of the sugars glucose, galactose or fructose, which prevents proper digestion of these molecules and larger molecules made from them. It may cause osmotic diarrhoea.

Exclusions from above levels

3A10.Z – Hereditary haemolytic anaemia due to enzyme deficiency
5A71.01 – Congenital adrenal hyperplasia
5A81.1 – 5-alpha-reductase deficiency

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LD28.01 – Marfan syndrome
LD28.1 – Ehlers-Danlos syndrome
LD2A.4 – androgen resistance syndrome
18 – Pregnancy, childbirth or the puerperium
http://id.who.int/icd/entity/1004987305 – Transitory endocrine or metabolic disorders specific to fetus or newborn

Child codes

5C61.40 – Fructose malabsorption
5C61.4Y – Other specified acquired monosaccharide malabsorption
5C61.4Z – Acquired monosaccharide malabsorption, unspecified

Sibling codes

5C61.0 – Glucose-galactose malabsorption
5C61.1 – Maltase-glucoamylase deficiency
5C61.2 – Congenital sucrase-isomaltase deficiency
5C61.3 – Alpha, alpha trehalase deficiency
5C61.5 – Disorders of facilitated glucose transport
5C61.6 – Lactose intolerance
5C61.Y – Other specified disorders of carbohydrate absorption or transport
5C61.Z – Disorders of carbohydrate absorption or transport, unspecified

Foundation entity

Acquired monosaccharide malabsorption – http://id.who.int/icd/entity/1361265641

Part of: 5C61: Disorders of carbohydrate absorption or transport › 05: Endocrine, nutritional or metabolic diseases