E70-E90
Metabolic disorders
E70
Disorders of aromatic amino- acid metabolism
E70.0
Primary diagnosis candidate
Classical phenylketonuria
E70.1
Primary diagnosis candidate
Other hyperphenylalanina emias
E70.2
Primary diagnosis candidate
Disorders of tyrosine metabolism
E70.3
Primary diagnosis candidate
Albinism
E70.8
Primary diagnosis candidate
Other disorders of aromatic amino- acid metabolism
E70.9
Primary diagnosis candidate
Disorder of aromatic amino- acid metabolism, unspecified
E71
Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
E71.0
Primary diagnosis candidate
Maple-syrup-urine disease
E71.1
Primary diagnosis candidate
Other disorders of branched-chain amino-acid metabolism
E71.2
Primary diagnosis candidate
Disorder of branched-chain amino-acid metabolism, unspecified
E71.3
Primary diagnosis candidate
Disorders of fatty- acid metabolism
E72
Other disorders of amino-acid metabolism
E72.0
Primary diagnosis candidate
Disorders of amino- acid transport
E72.1
Primary diagnosis candidate
Disorders of sulfur- bearing amino-acid metabolism
E72.2
Primary diagnosis candidate
Disorders of urea cycle metabolism
E72.3
Primary diagnosis candidate
Disorders of lysine and hydroxylysine metabolism
E72.4
Primary diagnosis candidate
Disorders of ornithine metabolism
E72.5
Primary diagnosis candidate
Disorders of glycine metabolism
E72.8
Primary diagnosis candidate
Other specified disorders of amino- acid metabolism
E72.9
Primary diagnosis candidate
Disorder of amino- acid metabolism, unspecified
E73
Lactose intolerance
E73.0
Primary diagnosis candidate
Congenital lactase deficiency
E73.1
Primary diagnosis candidate
Secondary lactase deficiency
E73.8
Primary diagnosis candidate
Other lactose intolerance
E73.9
Primary diagnosis candidate
Lactose intolerance, unspecified
E74
Other disorders of carbohydrate metabolism
E74.0
Primary diagnosis candidate
Glycogen storage disease
E74.1
Primary diagnosis candidate
Disorders of fructose metabolism
E74.2
Primary diagnosis candidate
Disorders of galactose metabolism
E74.3
Primary diagnosis candidate
Other disorders of intestinal carbohydrate absorption
E74.4
Primary diagnosis candidate
Disorders of pyruvate metabolism and gluconeogenesis
E74.8
Primary diagnosis candidate
Other specified disorders of carbohydrate metabolism
E74.9
Primary diagnosis candidate
Disorder of carbohydrate metabolism, unspecified
E75
Disorders of sphingolipid metabolism and other lipid storage disorders
E75.0
Primary diagnosis candidate
GM2 gangliosidosis Disease:
E75.1
Primary diagnosis candidate
Other gangliosidosis
E75.2
Primary diagnosis candidate
Other sphingolipidosis
E75.3
Primary diagnosis candidate
Sphingolipidosis, unspecified
E75.4
Primary diagnosis candidate
Neuronal ceroid lipofuscinosis
E75.5
Primary diagnosis candidate
Other lipid storage disorders
E75.6
Primary diagnosis candidate
Lipid storage disorder, unspecified
E76
Disorders of glycosaminoglycan metabolism
E76.0
Primary diagnosis candidate
Mucopolysaccharid osis, type I
E76.1
Primary diagnosis candidate
Mucopolysaccharid osis, type II
E76.2
Primary diagnosis candidate
Other mucopolysaccharido ses
E76.3
Primary diagnosis candidate
Mucopolysaccharid osis, unspecified
E76.8
Primary diagnosis candidate
Other disorders of glucosaminoglycan metabolism
E76.9
Primary diagnosis candidate
Disorder of glucosaminoglycan metabolism, unspecified
E77
Disorders of glycoprotein metabolism