autosomal dominant Alport syndrome
ORPHA: 88918
Overview
Alport syndrome that has material -basis in heterozygous mutation in the COL4A3 gene
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
Orphanet Code
ORPHA:88918autosomal dominant Alport syndrome
| Orphanet | ORPHA:88918 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO