hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
ORPHA: 251380
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 hereditary persistence of fetal hemoglobin-sickle cell disease syndrome, sourced from HPO and Orphanet clinical annotations.
Persistence of hemoglobin FHbS hemoglobinRetinopathySplenomegalyAspleniaReticulocytosisAbdominal painPulmonary infiltratesArthralgiaHypochromic microcytic anemiaIncreased red cell sickling tendencySevere infectionSplenic infarction
Classification & Codes
Orphanet Code
ORPHA:251380hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
| Orphanet | ORPHA:251380 |
| Treatments | 0 drug(s) |
| Symptoms on record | 13 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO