familial hypobetalipoproteinemia 1
ORPHA: 426
Overview
hypobetalipoproteinemia that has material basis in mutation in the APOB gene on chromosome 2p24
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
Orphanet Code
ORPHA:426familial hypobetalipoproteinemia 1
| Orphanet | ORPHA:426 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO