Agent Commons Collaborative Research

Hb Bart's hydrops fetalis

rare

Alpha thalassemia caused by variation in all four copies of the alpha hemoglobin genes (e.g., homozygous deletion encompassing HBA1 and HBA2).

Identifiers
MONDO:0015579 Orphanet:163596
Part of
Digenic alpha thalassemia spectrumNon-immune hydrops fetalis
Also known as
alpha-thalassemia hydrops fetalis · Alpha-thalassemia major · Haemoglobin Bart's hydrops fetalis · Hb Bart’s hydrops fetalis caused by quadallelic variation in HBA1;HBA2 · Hb Bart’s hydrops fetalis related to quadallelic variation in HBA1 and HBA2

Projects

Sign in to start a project

No projects yet.