Disorders of fructose metabolism

Description

This refers to disorders of the metabolism of fructose in the phosphorylation of fructose to fructose 1-phosphate by fructokinase, thus trapping fructose for metabolism in the liver.

Exclusions from above levels

5A41 – hypoglycaemia NOS
5A42 – Increased secretion of glucagon
5C56.3 – Mucopolysaccharidosis

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http://id.who.int/icd/entity/465177735 – Diabetes mellitus
http://id.who.int/icd/entity/1191191920 – Disorders of lipoprotein metabolism or certain specified lipidaemias
3A10.Z – Hereditary haemolytic anaemia due to enzyme deficiency
5A71.01 – Congenital adrenal hyperplasia
5A81.1 – 5-alpha-reductase deficiency
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

5C51.50 – Hereditary fructose intolerance
5C51.5Y – Other specified disorders of fructose metabolism
5C51.5Z – Disorders of fructose metabolism, unspecified

Foundation children elsewhere

5C61.40 – Fructose malabsorption

Sibling codes

5C51.0 – Disorders of the pentose phosphate pathway
5C51.1 – Disorders of glycerol metabolism
5C51.2 – Disorders of glyoxylate metabolism
5C51.3 – Glycogen storage disease
5C51.4 – Disorders of galactose metabolism
5C51.Y – Other specified inborn errors of carbohydrate metabolism
5C51.Z – Inborn errors of carbohydrate metabolism, unspecified

Foundation entity

Disorders of fructose metabolism – http://id.who.int/icd/entity/596254627

Part of: 5C51: Inborn errors of carbohydrate metabolism › 05: Endocrine, nutritional or metabolic diseases