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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
lipid storage disease
Summary
- Synonym
-
- Lipoid storage diseas
- inborn lipid storage disorder
- lipoidosis
- Definition
- A lysosomal storage disease that involves the accumulation of harmful amounts of lipids (fats) in some of the body's cells and tissues.
- Super Class
- lysosomal storage disease
External Links
- Disease Ontology
- DOID:9455
- Mondo Disease Ontology
- MeSH
- UMLS
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 3958 | LGALS3 | galectin 3 | |
| 3988 | LIPA | lipase A, lysosomal acid type | |
| 4023 | LPL | lipoprotein lipase | |
| 4047 | LSS | lanosterol synthase | |
| 4126 | MANBA | mannosidase beta | |
| 4668 | NAGA | alpha-N-acetylgalactosaminidase | |
| 4684 | NCAM1 | neural cell adhesion molecule 1 | |
| 4907 | NT5E | 5'-nucleotidase ecto | |
| 5476 | CTSA | cathepsin A | |
| 5660 | PSAP | prosaposin |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q13231 | Chitotriosidase-1 | |
| Q13510 | Acid ceramidase | |
| Q3T906 | N-acetylglucosamine-1-phosphotransferase subunits alpha/beta | |
| Q7L5L3 | Lysophospholipase D GDPD3 | |
| Q9UJJ9 | N-acetylglucosamine-1-phosphotransferase subunit gamma | |
| Q9UK23 | N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase |
