Maltase-glucoamylase deficiency

Description

Chronic diarrhea due to glucoamylase deficiency is characterised by chronic diarrhoea in infancy or childhood in association with intestinal glucoamylase deficiency.

Index terms

Maltase-glucoamylase deficiency
Chronic diarrhoea due to glucoamylase deficiency

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

5C61.0 – Glucose-galactose malabsorption
5C61.2 – Congenital sucrase-isomaltase deficiency
5C61.3 – Alpha, alpha trehalase deficiency
5C61.4 – Acquired monosaccharide malabsorption
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

Maltase-glucoamylase deficiency – http://id.who.int/icd/entity/2084206046

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