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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 |
|---|---|---|---|
| 142 | PARP1 | poly(ADP-ribose) polymerase 1 | |
| 1545 | CYP1B1 | cytochrome P450 family 1 subfamily B member 1 | |
| 1646 | AKR1C2 | aldo-keto reductase family 1 member C2 | |
| 2026 | ENO2 | enolase 2 | |
| 3283 | HSD3B1 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1 | |
| 3383 | ICAM1 | intercellular adhesion molecule 1 | |
| 3635 | INPP5D | inositol polyphosphate-5-phosphatase D | |
| 5315 | PKM | pyruvate kinase M1/2 | |
| 5621 | PRNP | prion protein (Kanno blood group) | |
| 5728 | PTEN | phosphatase and tensin homolog |
Related Glycoprotein
