| LAL | left axillary line; Limulus amebocyte lysate; low air loss; lysosomal acid lipase |
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| LAL | Lysosomal acid lipase |
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| LAP | Lysosomal acid phosphatase |
| LSD | Lysosomal storage diseases |
| ML | mitochondrial lysosomal |
| lysosomal disease | A disease due to inadequate functioning of a lysosomal enzyme; most such disease's are associated with a storage disease. (05 Mar 2000) |
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| lysosomal diseases | 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. (18 Nov 1997) |
| lysosomal enzyme | <biochemistry> A range of degradative enzymes, most of which operate best at acid pH. The best known marker enzymes are acid phosphatase and glucuronidase, but many others are known. (18 Nov 1997) |
| lysosomal storage diseases | Inborn errors of metabolism characterised by defects in specific lysosomal hydrolases and resulting in intracellular accumulation of unmetabolised substrates. (12 Dec 1998) |
| inborn lysosomal disease | Inherited disorder of one or more degradative enzymes normally located in lysosomes leading to accumulation (storage) of abnormal quantities of a substance, such as a glycosaminoglycan as in Hurler's syndrome or a lipopolysaccharide as in Gaucher's disease. (05 Mar 2000) |
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| UDP-N-acetylglucosamine-lysosomal-enzyme-N-acetylglucosaminephosphotransferase | <enzyme> Fibroblasts from patients with i-cell (mucolipidosis II) and pseudo-hurler polydystrophy (mucolipidosis III) are deficient in above enzyme; for n-acetylglucosamine transferred to dolichyl phosphate see EC 2.7.8.15 Registry number: EC 2.7.8.17 Synonym: udpgnac gp gnac phosphotransferase, udpgnac phosphotransferase, uridine 5'-diphosphate-n-acetylglucosamine glycoprotein n-acetylglucosaminylphosphotransferase, n-acetylglucosamine-1-phosphotransferase, n-agapt, udp-n-acetylglucosamine-lysosomal glycoprotein n-acetylglucosaminylphosphotransferase, udp-acetylglucosamine-glycoprotein n-acetylglucosamine-1-phosphotransferase (26 Jun 1999) |
| UDP-N-acetylglucosamine:lysosomal enzyme N-acetylglucosaminyl-1-phosphotransferase | <enzyme> An enzyme that participates in the posttranslational modification of a number of lysosomal proteins; a deficiency or defect in this enzyme results in two forms of mucolipidoses, I-cell disease, and pseudo-Hurler polydystrophy. (05 Mar 2000) |
Synonyms : Disease, Lysosomal Storage, Diseases, Lysosomal Storage, Disorder, Lysosomal Enzyme, Disorders, Lysosomal Enzyme, Enzyme Disorder, Lysosomal, Enzyme Disorders, Lysosomal, Lysosomal Enzyme Disorder, Lysosomal Storage Disease
Synonyms : Lysosomal Enzyme Disorders, Nervous System, Nervous System Lysosomal Enzyme Disorders
Synonyms : CD107a Antigen, LAMP1 Protein, LAMPA Protein, LGP120 Protein, Lysosomal Associated Membrane Protein 1
Synonyms : CD107b Antigen, LAMP2 Protein, LGP-B Protein, LGP110 Protein, LGP B Protein, Lysosomal Associated Membrane Protein 2
| lysosomal storage disease |
An inherited disease characterized by a defect in the functional expression of any of the lysosomal enzymes.
Ãâó: www.lsdn.com/glance_glossary.shtml
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| lysosomal storage disease |
A disease caused by deficiency of specific lysosomal enzymes that normally degrade glycoproteins, glycolipids, or mucopolysaccharides. Thus, the substances that cannot be catabolized accumulate in lysosomes. Specific en
Ãâó:
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| lysosomal |
of or pertaining to a lysosome.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| lysosomal α-glucosidase |
glucan 1,4-α-glucosidase.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| lysosomal α-glucosidase deficiency |
glycogen storage disease, type II.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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