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arteriolosclerosis
Summary
- Definition
- An arteriosclerosis that is characterized by thickening of the wall of the small arteries and arterioles, caused by deposition of hyaline material in the wall or concentric smooth muscle wall hypertrophy, and results in lumen narrowing and tissue ischemia.
- Super Class
- arteriosclerosis
External Links
- Disease Ontology
- DOID:5162
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 81579 | PLA2G12A | phospholipase A2 group XIIA | |
| 93589 | CACNA2D4 | calcium voltage-gated channel auxiliary subunit alpha2delta 4 | |
| 93978 | CLEC6A | C-type lectin domain containing 6A | |
| 151056 | PLB1 | phospholipase B1 | |
| 166929 | SGMS2 | sphingomyelin synthase 2 | |
| 259230 | SGMS1 | sphingomyelin synthase 1 | |
| 283420 | CLEC9A | C-type lectin domain containing 9A | |
| 338328 | GPIHBP1 | glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1 | |
| 339221 | ENPP7 | ectonucleotide pyrophosphatase/phosphodiesterase 7 | |
| 340075 | ARSI | arylsulfatase family member I |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P23786 | Carnitine O-palmitoyltransferase 2, mitochondrial | |
| P24557 | Thromboxane-A synthase | |
| P24752 | Acetyl-CoA acetyltransferase, mitochondrial | |
| P26718 | NKG2-D type II integral membrane protein | |
| P27797 | Calreticulin | |
| P27824 | Calnexin | |
| P28845 | 11-beta-hydroxysteroid dehydrogenase 1 | |
| P31431 | Syndecan-4 | |
| P33121 | Long-chain-fatty-acid--CoA ligase 1 | |
| P34913 | Bifunctional epoxide hydrolase 2 |
