E71.541 Zellweger-like syndrome |
E71.542 Other group 3 peroxisomal disorders |
E71.548 Other peroxisomal disorders |
E72.00 Disorders of amino-acid transport, unspecified |
E72.01 Cystinuria |
E72.02 Hartnup's disease |
E72.03 Lowe's syndrome |
E72.04 Cystinosis |
E72.09 Other disorders of amino-acid transport |
E72.10 Disorders of sulfur-bearing amino-acid metabolism, unspecified |
E72.11 Homocystinuria |
E72.12 Methylenetetrahydrofolate reductase deficiency |
E72.19 Other disorders of sulfur-bearing amino-acid metabolism |
E72.20 Disorder of urea cycle metabolism, unspecified |
E72.21 Argininemia |
E72.22 Arginosuccinic aciduria |
E72.23 Citrullinemia |
E72.29 Other disorders of urea cycle metabolism |
E72.3 Disorders of lysine and hydroxylysine metabolism |
E72.4 Disorders of ornithine metabolism |
E72.50 Disorder of glycine metabolism, unspecified |
E72.51 Non-ketotic hyperglycinemia |
E72.52 Trimethylaminuria |
E72.53 Primary hyperoxaluria |
E72.59 Other disorders of glycine metabolism |
E72.81 Disorders of gamma aminobutyric acid metabolism |
E72.89 Other specified disorders of amino-acid metabolism |
E72.9 Disorder of amino-acid metabolism, unspecified |
E73.0 Congenital lactase deficiency |
E73.1 Secondary lactase deficiency |
E73.8 Other lactose intolerance |
E73.9 Lactose intolerance, unspecified |
E74.00 Glycogen storage disease, unspecified |
E74.01 von Gierke disease |
E74.02 Pompe disease |
E74.03 Cori disease |
E74.04 McArdle disease |
E74.09 Other glycogen storage disease |
E74.10 Disorder of fructose metabolism, unspecified |
E74.11 Essential fructosuria |
E74.12 Hereditary fructose intolerance |
E74.19 Other disorders of fructose metabolism |
E74.20 Disorders of galactose metabolism, unspecified |
E74.21 Galactosemia |
E74.29 Other disorders of galactose metabolism |
E74.31 Sucrase-isomaltase deficiency |
E74.39 Other disorders of intestinal carbohydrate absorption |
E74.4 Disorders of pyruvate metabolism and gluconeogenesis |
E74.810 Glucose transporter protein type 1 deficiency |
E74.818 Other disorders of glucose transport |
E74.819 Disorders of glucose transport, unspecified |
E74.89 Other specified disorders of carbohydrate metabolism |
E74.9 Disorder of carbohydrate metabolism, unspecified |
E75.00 GM2 gangliosidosis, unspecified |
E75.01 Sandhoff disease |
E75.02 Tay-Sachs disease |
E75.09 Other GM2 gangliosidosis |
E75.10 Unspecified gangliosidosis |
E75.11 Mucolipidosis IV |
E75.19 Other gangliosidosis |
E75.21 Fabry (-Anderson) disease |
E75.22 Gaucher disease |
E75.23 Krabbe disease |
E75.240 Niemann-Pick disease type A |
E75.241 Niemann-Pick disease type B |
E75.242 Niemann-Pick disease type C |
E75.243 Niemann-Pick disease type D |
E75.244 Niemann-Pick disease type A/B |
E75.248 Other Niemann-Pick disease |
E75.249 Niemann-Pick disease, unspecified |
E75.25 Metachromatic leukodystrophy |
E75.26 Sulfatase deficiency |
E75.29 Other sphingolipidosis |
E75.3 Sphingolipidosis, unspecified |
E75.4 Neuronal ceroid lipofuscinosis |
E75.5 Other lipid storage disorders |
E75.6 Lipid storage disorder, unspecified |
E76.01 Hurler's syndrome |
E76.02 Hurler-Scheie syndrome |
E76.03 Scheie's syndrome |
E76.1 Mucopolysaccharidosis, type II |
E76.210 Morquio A mucopolysaccharidoses |
E76.211 Morquio B mucopolysaccharidoses |
E76.219 Morquio mucopolysaccharidoses, unspecified |
E76.22 Sanfilippo mucopolysaccharidoses |
E76.29 Other mucopolysaccharidoses |
E76.3 Mucopolysaccharidosis, unspecified |
E76.8 Other disorders of glucosaminoglycan metabolism |
E76.9 Glucosaminoglycan metabolism disorder, unspecified |
E77.0 Defects in post-translational modification of lysosomal enzymes |
E77.1 Defects in glycoprotein degradation |
E77.8 Other disorders of glycoprotein metabolism |
E77.9 Disorder of glycoprotein metabolism, unspecified |
E78.00 Pure hypercholesterolemia, unspecified |
E78.01 Familial hypercholesterolemia |
E78.1 Pure hyperglyceridemia |
E78.2 Mixed hyperlipidemia |
E78.3 Hyperchylomicronemia |
E78.41 Elevated Lipoprotein(a) |
E78.49 Other hyperlipidemia |