5C56.0Y Other specified sphingolipidosis

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

synonyms

• Other specified sphingolipidosis
• Mucolipidosis type 4
• Sialolipidosis
• Gaucher disease
• Acid beta-glucosidase deficiency
• Glucocerebrosidase deficiency
• Glucosylceramide beta-glucosidase deficiency
• Glucocerebrosidosis
• Cerebroside lipidosis syndrome
• Gaucher disease type 1
• Noncerebral juvenile Gaucher disease
• Adult Gaucher disease
• Gaucher disease type 2
• Acute neuronopathic Gaucher disease
• Infantile cerebral Gaucher disease
• Infantile Gaucher disease
• Cerebral acute Gaucher disease
• Gaucher disease type 3
• Cerebral juvenile and adult form of Gaucher disease
• Chronic neuronopathic Gaucher disease
• Subacute neuronopathic Gaucher disease
• Juvenile Gaucher disease
• Norrbotnian Gaucher disease
• Gaucher disease - ophthalmoplegia - cardiovascular calcification
• Cardiovascular Gaucher disease
• Gaucher disease type 3C
• Gaucher-like disease
• Perinatal-lethal Gaucher disease
• Fetal Gaucher disease
• Collodion type Gaucher disease
• Atypical Gaucher disease due to saposin C deficiency
• Gaucher’s splenomegaly
• Mucosulfatidosis
• Multiple sulfatase deficiency
• Juvenile sulfatidose, Austin type
• Austin disease
• Niemann-Pick disease
• Sphingomyelinase deficiency
• Niemann-Pick disease type A
• Niemann-Pick disease type B
• Niemann-Pick disease type C
• cholesterol transporter deficiency
• Niemann-Pick disease type C, severe perinatal
• Niemann-Pick disease type C, severe early infantile neurologic onset
• Niemann-Pick disease type C, late infantile neurologic onset
• Niemann-Pick disease type C, juvenile neurologic onset
• Niemann-Pick disease type C, classic form
• Niemann-Pick disease type C, adult neurologic onset
• Farber disease
• Farber lipogranulomatosis
• Ceramidase deficiency
• Disseminated lipogranulomatosis
• Lysosomal acid lipase deficiency
• Acid esterase deficiency
• Wolman disease
• Cholesteryl ester storage disease
• CESD - [Cholesteryl ester storage disease]
• Encephalopathy due to prosaposin deficiency
• Combined prosaposin deficiency

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