Certain infectious and parasitic diseases
Certain infectious and parasitic diseases Certain infectious and parasitic diseases
E75 Disorders of sphingolipid metabolism and other lipid storage disorders Excludes: mucolipidosis, types I-III ( E77.0-E77.1 ) Refsum's disease ( G60.1 ) E75.0 GM 2 gangliosidosis Disease: · Sandhoff · Tay-Sachs GM 2 gangliosidosis: · NOS · adult · juvenile E75.1 Other gangliosidosis Gangliosidosis: · NOS · GM 1 · GM 3 Mucolipidosis IV E75.2 Other sphingolipidosis Disease: · Fabry(-Anderson) · Gaucher · Krabbe · Niemann-Pick Faber's syndrome Metachromatic leukodystrophy Sulfatase deficiency Excludes: adrenoleukodystrophy [Addison-Schilder] ( E71.3 ) E75.3 Sphingolipidosis, unspecified E75.4 Neuronal ceroid lipofuscinosis Disease: · Batten · Bielschowsky-Jansky · Kufs · Spielmeyer-Vogt E75.5 Other lipid storage disorders Cerebrotendinous cholesterosis [van Bogaert-Scherer-Epstein] Wolman's disease E75.6 Lipid storage disorder, unspecified 162 WHO’s ICD-10
E76 Disorders of glycosaminoglycan metabolism E76.0 Mucopolysaccharidosis, type I Syndrome: · Hurler · Hurler-Scheie · Scheie E76.1 Mucopolysaccharidosis, type II Hunter's syndrome E76.2 Other mucopolysaccharidoses Beta-glucuronidase deficiency Mucopolysaccharidosis, types III, IV, VI, VII Syndrome: · Maroteaux-Lamy (mild)(severe) · Morquio(-like)(classic) · Sanfilippo (type B)(type C)(type D) E76.3 Mucopolysaccharidosis, unspecified E76.8 Other disorders of glucosaminoglycan metabolism E76.9 Disorder of glucosaminoglycan metabolism, unspecified E77 Disorders of glycoprotein metabolism E77.0 Defects in post-translational modification of lysosomal enzymes Mucolipidosis II [I-cell disease] Mucolipidosis III [pseudo-Hurler polydystrophy] E77.1 Defects in glycoprotein degradation Aspartylglucosaminuria Fucosidosis Mannosidosis Sialidosis [mucolipidosis I] E77.8 Other disorders of glycoprotein metabolism E77.9 Disorder of glycoprotein metabolism, unspecified E78 Disorders of lipoprotein metabolism and other lipidaemias Excludes: sphingolipidosis ( E75.0-E75.3 ) E78.0 Pure hypercholesterolaemia Familial hypercholesterolaemia Fredrickson's hyperlipoproteinaemia, type IIa Hyperbetalipoproteinaemia Hyperlipidaemia, group A Low-density-lipoprotein-type [LDL] hyperlipoproteinaemia E78.1 Pure hyperglyceridaemia Endogenous hyperglyceridaemia Fredrickson's hyperlipoproteinaemia, type IV Hyperlipidaemia, group B Hyperprebetalipoproteinaemia Very-low-density-lipoprotein-type [VLDL] hyperlipoproteinaemia Version for 2007 163
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E76 Disorders of glycosaminoglycan metabolism<br />
E76.0 Mucopolysaccharidosis, type I<br />
Syndrome:<br />
· Hurler<br />
· Hurler-Scheie<br />
· Scheie<br />
E76.1 Mucopolysaccharidosis, type II<br />
Hunter's syndrome<br />
E76.2 Other mucopolysaccharidoses<br />
Beta-glucuronidase deficiency<br />
Mucopolysaccharidosis, types III, IV, VI, VII<br />
Syndrome:<br />
· Maroteaux-Lamy (mild)(severe)<br />
· Morquio(-like)(classic)<br />
· Sanfilippo (type B)(type C)(type D)<br />
E76.3 Mucopolysaccharidosis, unspecified<br />
E76.8 Other disorders of glucosaminoglycan metabolism<br />
E76.9 Disorder of glucosaminoglycan metabolism, unspecified<br />
E77 Disorders of glycoprotein metabolism<br />
E77.0 Defects in post-translational modification of lysosomal enzymes<br />
Mucolipidosis II [I-cell disease]<br />
Mucolipidosis III [pseudo-Hurler polydystrophy]<br />
E77.1 Defects in glycoprotein degradation<br />
Aspartylglucosaminuria<br />
Fucosidosis<br />
Mannosidosis<br />
Sialidosis [mucolipidosis I]<br />
E77.8 Other disorders of glycoprotein metabolism<br />
E77.9 Disorder of glycoprotein metabolism, unspecified<br />
E78 Disorders of lipoprotein metabolism <strong>and</strong> other lipidaemias<br />
Excludes: sphingolipidosis ( E75.0-E75.3 )<br />
E78.0 Pure hypercholesterolaemia<br />
Familial hypercholesterolaemia<br />
Fredrickson's hyperlipoproteinaemia, type IIa<br />
Hyperbetalipoproteinaemia<br />
Hyperlipidaemia, group A<br />
Low-density-lipoprotein-type [LDL] hyperlipoproteinaemia<br />
E78.1 Pure hyperglyceridaemia<br />
Endogenous hyperglyceridaemia<br />
Fredrickson's hyperlipoproteinaemia, type IV<br />
Hyperlipidaemia, group B<br />
Hyperprebetalipoproteinaemia<br />
Very-low-density-lipoprotein-type [VLDL] hyperlipoproteinaemia<br />
Version for 2007 163
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