Medical

cerebroside lipoidosis

cer·ebr·o·side lip·oi·do·sis

a group of lysosomal storage diseases characterized by accumulation of lipid in cells of affected tissue and commonly accompanied by a manifest derangement of central nervous system development; for example, Gaucher disease and Krabbe disease.

All content on this website, including dictionary, thesaurus, literature, geography, and other reference data is for informational purposes only. This information should not be considered complete, up to date, and is not intended to be used in place of a visit, consultation, or advice of a legal, medical, or any other professional.