ICD9 Online Home

Free online searchable
2009 ICD-9-CM

Search for  

Diseases and Injuries
>> Tabular Index
>> Alphabetic Index

Procedures
>> Tabular Index
>> Alphabetic Index

Appendices
>> Drugs / Chemicals
>> External Causes

Other Resources
>> HCPCS Alpha
>> Medical Dictionary
>> Drug Directory


Tips
Contribute




Xanthomatosis, Cerebrotendinous

Van Bogaert-Scherer-Epstein Disease | Bogaert-Scherer-Epstein Disease, Van | Cerebrotendinous Xanthomatoses | Cerebrotendinous Xanthomatosis | Disease, Van Bogaert-Scherer-Epstein | Van Bogaert Scherer Epstein Disease

A lipid storage disease, inherited as an autosomal recessive trait, characterized by xanthomas of the tendons, the white matter of the brain, and the lungs, and by spasticity, ataxia, pyramidal paresis, mental retardation, dementia, early cataracts, and atherosclerosis. It is associated with elevated plasma and tissue levels of cholestanol and defective bile synthesis, with the deposition of cholestanol in the central nervous system and myelin of peripheral nerves. The lesions contain cholesterol and dehydrocholesterol. (Dorland, 28th ed)
 
Google
 
Web icd9cm.chrisendres.com