Skyscape Web Viewer : International Classification of Diseases : ICD10 Index

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[E75.5]-Van Bogaert-Scherer-Epstein disease or syndrome
[E75.5]-Wolman's disease
[E75.6] - Lipid storage disorder, unspecified
[E75] - Disorders of sphingolipid metabolism and other lipid storage disorders
[E76.0] - Mucopolysaccharidosis, type I
[E76.01]-Gargoylism
[E76.01] - Hurler's syndrome
[E76.01]-Lipochondrodystrophy
[E76.02]-Hurler (-Scheie) disease or syndrome
[E76.02] - Hurler-Scheie syndrome
[E76.03] - Scheie's syndrome
[E76.03]-Scheie's syndrome
[E76.1] - Mucopolysaccharidosis, type II
[E76.2] - Other mucopolysaccharidoses
[E76.21] - Morquio mucopolysaccharidoses
[E76.210] - Morquio A mucopolysaccharidoses
[E76.211] - Morquio B mucopolysaccharidoses
[E76.219]-Chondro-osteodysplasia (Morquio-Brailsford type)
[E76.219] - Morquio mucopolysaccharidoses, unspecified
[E76.22]-Sanfilippo (Type B) (Type C) (Type D) syndrome
[E76.22] - Sanfilippo mucopolysaccharidoses
[E76.29]-Chondro-osteodystrophy
[E76.29]-Eccentro-osteochondrodysplasia
[E76.29]-Maroteaux-Lamy syndrome (mild) (severe)
[E76.29] - Other mucopolysaccharidoses
[E76.3] - Mucopolysaccharidosis, unspecified
[E76.8] - Other disorders of glucosaminoglycan metabolism
[E76.9] - Glucosaminoglycan metabolism disorder, unspecified
[E76] - Disorders of glycosaminoglycan metabolism
[E77.0] - Defects in post-translational modification of lysosomal enzymes