hemoglobin variants
Hemoglobin variants refer to genetic mutations that cause structural changes in the protein hemoglobin, leading to different forms or types of this essential molecule found in red blood cells.
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Related Concepts (25)
- fetal hemoglobin (hbf)
- glycated hemoglobin
- hba1c
- hemoglobin a1c (hba1c) test
- hemoglobin c disease
- hemoglobin d trait
- hemoglobin e (hbe) disease
- hemoglobin electrophoresis
- hemoglobin e–thalassemia syndrome
- hemoglobin h disease
- hemoglobin lepore trait
- hemoglobin m disease
- hemoglobin s-c disease
- hemoglobin variants and blood transfusion complications
- hemoglobin variants and differential diagnosis
- hemoglobin variants and prevalence in newborn screening
- hemoglobin variants and sickle cell trait
- hemoglobin variants and their clinical significance
- hemoglobin variants and their impact on health
- hemoglobin variants in different populations
- hemoglobinopathies
- hemoglobinopathies and oxidative stress
- hemoglobinopathies in pregnancy
- sickle cell anemia
- thalassemia
Similar Concepts
- blood genetic testing
- blood types
- dna sequence variation
- gene mutation
- gene mutations
- gene variants and type 2 diabetes
- genetic polymorphism
- genetic variation in the human genome
- genetic variations
- genetic variations influencing prediabetes risk
- haplotypes
- hemoglobin a1c
- hemoglobin a1c testing
- polymorphisms in human genetics
- species variation