familial erythrocytosis 1
ORPHA: 90042
Overview
Human disease
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 familial erythrocytosis 1, sourced from HPO and Orphanet clinical annotations.
EpistaxisPruritusAbnormal bleedingPolycythemiaThromboembolismAbdominal painDyspneaHeadacheVertigoArthralgiaExertional dyspneaVenous thrombosisAbnormal hemoglobinFatigueCough
Classification & Codes
Orphanet Code
ORPHA:90042familial erythrocytosis 1
| Orphanet | ORPHA:90042 |
| Treatments | 0 drug(s) |
| Symptoms on record | 15 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO