Search for a gene
HBA2 - hemoglobin subunit alpha 2
- Disease-causing germline mutation(s) in Autosomal dominant secondary polycythemia
- Disease-causing germline mutation(s) in Hb Bart's hydrops fetalis
- Disease-causing germline mutation(s) in Hemoglobin H disease
- Disease-causing germline mutation(s) in Hemoglobin M disease
- Role in the phenotype of Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
Orphanet is part of the Gene Curation Coalition, a global effort to harmonise gene-level resources.