Acquired monosaccharide malabsorption, unspecified

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

Sibling codes

5C61.40 – Fructose malabsorption
5C61.4Y – Other specified acquired monosaccharide malabsorption

Foundation entity

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

Part of: 5C61.4: Acquired monosaccharide malabsorption › 5C61: Disorders of carbohydrate absorption or transport › 05: Endocrine, nutritional or metabolic diseases