Niemann-Pick disease

Summary
Synonym
  • Sphingomyelinase Deficiency Disease
  • lipoid histiocytosis
  • sphingomyelin lipidosis
Definition
A sphingoliidosis characterized by the accumulation of the lipid sphingomyelin in lysosomes in cells.
Super Class
sphingolipidosis
External Links
Disease Ontology
DOID:14504
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 21 - 30 of 30 in total
Gene ID Gene Symbol Description Source
5660 PSAP prosaposin
6609 SMPD1 sphingomyelin phosphodiesterase 1
6610 SMPD2 sphingomyelin phosphodiesterase 2
7357 UGCG UDP-glucose ceramide glucosyltransferase
8869 ST3GAL5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5
8879 SGPL1 sphingosine-1-phosphate lyase 1
10724 OGA O-GlcNAcase
10924 SMPDL3A sphingomyelin phosphodiesterase acid like 3A
57704 GBA2 glucosylceramidase beta 2
132789 GNPDA2 glucosamine-6-phosphate deaminase 2
Displaying all 2 entries
Gene ID Gene Symbol Description Source
18145 Npc1 NPC intracellular cholesterol transporter 1
20597 Smpd1 sphingomyelin phosphodiesterase 1, acid lysosomal
Displaying all 3 entries
Gene ID Gene Symbol Description Source
174131 asm-1 Sphingomyelin phosphodiesterase 1
176879 asm-3 Putative sphingomyelin phosphodiesterase asm-3;Sphingomyelin phosphodiesterase
181323 asm-2 Sphingomyelin phosphodiesterase 2
Related Glycoprotein

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024