familial hyperinsulinism
ORPHA: 276525
Overview
instance of hyperinsulinism (disease) that is caused by an inherited modification of the individual's genome
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
Orphanet Code
ORPHA:276525familial hyperinsulinism
| Orphanet | ORPHA:276525 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO