alpha thalassemia

MeSH: D017085ORPHA: 846

Overview

thalassemia involving the hemoglobin genes HBA1 and HBA2

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 alpha thalassemia, sourced from HPO and Orphanet clinical annotations.

CholelithiasisSplenomegalyHydrops fetalisHemolytic anemiaAnemiaHypersplenismMyelodysplasiaAnisopoikilocytosisHemoglobin BartsMalar prominenceAbnormality of immune system physiologyCognitive impairmentHyperplasia of the maxillaMicrocytic anemiaAbnormal hemoglobinHepatosplenomegalyCongestive heart failurePericardial effusionReticulocytosisExtramedullary hematopoiesisPleural effusionGeneralized edemaJaundice

Classification & Codes

MeSH Code

D017085

Orphanet Code

ORPHA:846
alpha thalassemia
MeSHD017085
OrphanetORPHA:846
Treatments0 drug(s)
Symptoms on record23 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO