Medical Definition of Lysosomal diseases

1. Diseases (also called storage diseases) in which a deficiency of a particular lysosomal enzyme leads to accumulation of the undigested substrate for that enzyme within cells. Not immediately fatal, but within a few years lead to serious neurological and skeletal disorders and eventually to death. See: the following conditions: Hurler sundrome, Hunter syndrome, San Fillipo, Gaucher's disease, Niemann-Pick, Pompe's disease, Tay Sachs disease. This entry appears with permission from the Dictionary of Cell and Molecular Biology (11 Mar 2008)

Lexicographical Neighbors of Lysosomal Diseases

lysomonogalactosyldiacylglycerol acyltransferase
lysophosphatide
lysophosphatidic acid
lysophosphatidic acid-hydrolysing lysophospholipase
lysophosphatidic acid acyltransferase
lysophosphatidic acid phosphatase
lysophosphatidylcholine
lysophosphatidylcholines
lysophosphatidylserine
lysophospholipase
lysophospholipase-transacylase
lysophospholipids
lysosogenic bacteriophage
lysosomal
lysosomal disease
lysosomal diseases (current term)
lysosomal enzyme
lysosomal storage diseases
lysosome
lysosome
lysosomes
lysosomes
lysosome associated membrane glycoprotein
lysosome phagosome fusion
lysostaphin
lysostaphin endopeptidase
lysotype
lysozyme
lysozyme
lysozymes

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