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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E75 Disorders of sphingolipid metabolism <strong>and</strong> other lipid storage<br />
disorders<br />
Excludes: mucolipidosis, types I-III ( E77.0-E77.1 )<br />
Refsum's disease ( G60.1 )<br />
E75.0 GM 2 gangliosidosis<br />
Disease:<br />
· S<strong>and</strong>hoff<br />
· Tay-Sachs<br />
GM 2 gangliosidosis:<br />
· NOS<br />
· adult<br />
· juvenile<br />
E75.1 Other gangliosidosis<br />
Gangliosidosis:<br />
· NOS<br />
· GM 1<br />
· GM 3<br />
Mucolipidosis IV<br />
E75.2 Other sphingolipidosis<br />
Disease:<br />
· Fabry(-Anderson)<br />
· Gaucher<br />
· Krabbe<br />
· Niemann-Pick<br />
Faber's syndrome<br />
Metachromatic leukodystrophy<br />
Sulfatase deficiency<br />
Excludes: adrenoleukodystrophy [Addison-Schilder] ( E71.3 )<br />
E75.3 Sphingolipidosis, unspecified<br />
E75.4 Neuronal ceroid lipofuscinosis<br />
Disease:<br />
· Batten<br />
· Bielschowsky-Jansky<br />
· Kufs<br />
· Spielmeyer-Vogt<br />
E75.5 Other lipid storage disorders<br />
Cerebrotendinous cholesterosis [van Bogaert-Scherer-Epstein]<br />
Wolman's disease<br />
E75.6 Lipid storage disorder, unspecified<br />
162 WHO’s ICD-10
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