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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 |
|---|---|---|
| P07098 | Gastric triacylglycerol lipase | |
| P07911 | Uromodulin | |
| P08236 | Beta-glucuronidase | |
| P10253 | Lysosomal alpha-glucosidase | |
| P10619 | Lysosomal protective protein | |
| P11169 | Solute carrier family 2, facilitated glucose transporter member 3 | |
| P11413 | Glucose-6-phosphate 1-dehydrogenase | |
| P13591 | Neural cell adhesion molecule 1 | |
| P14410 | Sucrase-isomaltase, intestinal | |
| P15289 | Arylsulfatase A |
