E75.2 Other sphingolipidosisNon-billable header with 9 child codes.
E75.21 Fabry (-Anderson) diseaseE75.22 Gaucher diseaseE75.23 Krabbe diseaseE75.24 Niemann-Pick diseaseE75.25 Metachromatic leukodystrophyE75.26 Sulfatase deficiencyE75.27 Pelizaeus-Merzbacher diseaseE75.28 Canavan diseaseE75.29 Other sphingolipidosisE78 Disorders of lipoprotein metabolism and other lipidemias ("sphingolipidosis (E75.0-E75.3)")G11 Hereditary ataxia ("metabolic disorders (E70-E88)")G63 Polyneuropathy in diseases classified elsewhere ("metabolic diseases (E70-E88)")G71 Primary disorders of muscles ("metabolic disorders (E70-E88)")G73.7 Myopathy in diseases classified elsewhere ("lipid storage disorders (E75.-)")H36 Retinal disorders in diseases classified elsewhere ("lipid storage disorders (E75.-)")H42 Glaucoma in diseases classified elsewhere ("specified metabolic disorder (E70-E88)")N25.0 Renal osteodystrophy ("metabolic disorders classifiable to E70-E88")N25.81 Secondary hyperparathyroidism of renal origin ("metabolic disorders classifiable to E70-E88")P59 Neonatal jaundice from other and unspecified causes ("jaundice due to inborn errors of metabolism (E70-E88)")R79 Other abnormal findings of blood chemistry ("specific findings indicating disorder of lipid metabolism (E75.-)")E75.09 Other GM2 gangliosidosisE75.1 Other and unspecified gangliosidosisE75.10 Unspecified gangliosidosisE75.11 Mucolipidosis IVE75.19 Other gangliosidosisE75.2 Other sphingolipidosis (this code)E75.21 Fabry (-Anderson) diseaseE75.22 Gaucher diseaseE75.23 Krabbe diseaseE75.24 Niemann-Pick diseaseE75.240 Niemann-Pick disease type A