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primary cutaneous amyloidosis
Summary
- Synonym
-
- PCA
- familial primary localized cutaneous amyloidosis
- Definition
- An amyloidosis characterized by pruritus, skin scratching and by deposits of amyloid in the dermis.
- Super Class
- amyloidosis inherited metabolic disorder skin disease
External Links
- Disease Ontology
- DOID:0050639
- Mondo Disease Ontology
- ORDO
- OMIM
- GARD
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 5743 | PTGS2 | prostaglandin-endoperoxide synthase 2 | |
| 6715 | SRD5A1 | steroid 5 alpha-reductase 1 | |
| 7355 | SLC35A2 | solute carrier family 35 member A2 | |
| 7367 | UGT2B17 | UDP glucuronosyltransferase family 2 member B17 | |
| 7512 | XPNPEP2 | X-prolyl aminopeptidase 2 | |
| 8809 | IL18R1 | interleukin 18 receptor 1 | |
| 9254 | CACNA2D2 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | |
| 23600 | AMACR | alpha-methylacyl-CoA racemase | |
| 27306 | HPGDS | hematopoietic prostaglandin D synthase | |
| 29956 | CERS2 | ceramide synthase 2 |
Related Glycoprotein
