hereditary cystatin C amyloid angiopathy
ORPHA: 100008
Overview
a cerebral amyloid angiopathy that has material basis in an autosomal dominant mutation of CST3 on chromosome 20p11.21.
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with hereditary cystatin C amyloid angiopathy, sourced from HPO and Orphanet clinical annotations.
StrokeCerebral hemorrhageAmyloid depositionCerebral amyloid angiopathy
Classification & Codes
Orphanet Code
ORPHA:100008hereditary cystatin C amyloid angiopathy
| Orphanet | ORPHA:100008 |
| Treatments | 0 drug(s) |
| Symptoms on record | 4 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO