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 gangliosidosis
 * E75.2 Other sphingolipidosis
 * Excludes1: adrenoleukodystrophy [Addison-Schilder] (E71.30)
 * E75.21 Fabry (-Anderson) disease
 * E75.22 Gaucher disease
 * E75.23 Krabbe disease
 * E75.24 Niemann-Pick 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
 * E75.248 Other Niemann-Pick disease
 * E75.249 Niemann-Pick disease, unspecified
 * E75.25 Metachromatic leukodystrophy
 * E75.29 Other sphingolipidosis
 * Farber's syndrome
 * Sulfatase deficiency
 * Sulfatide lipidosis
 * E75.3 Sphingolipidosis, unspecified
 * E75.4 Neuronal ceroid lipofuscinosis
 * Batten disease
 * Bielschowsky-Jansky disease
 * Kufs disease
 * Spielmeyer-Vogt disease
 * E75.5 Other lipid storage disorders
 * Cerebrotendinous cholesterosis [van Bogaert-Scherer-Epstein]
 * Wolman's disease
 * E75.6 Lipid storage disorder, unspecified

E76 Disorders of glycosaminoglycan metabolism

 * E76.0 Mucopolysaccharidosis, type I
 * E76.01 Hurler?s syndrome
 * E76.02 Hurler-Scheie syndrome
 * E76.03 Scheie?s syndrome
 * E76.1 Mucopolysaccharidosis, type II
 * Hunter's syndrome
 * E76.2 Other mucopolysaccharidoses
 * E76.21 Morquio mucopolysaccharidoses
 * E76.210 Morquio A mucopolysaccharidoses
 * Classic Morquio syndrome
 * Morquio syndrome A
 * Mucopolysaccharidosis, type IVA
 * E76.211 Morquio B mucopolysaccharidoses
 * Morquio-like mucopolysaccharidoses
 * Morquio-like syndrome
 * Morquio syndrome B
 * Mucopolysaccharidosis,