Final answer:
Thalassemia is the anemia described by the genetic defect in the beta chain of Hb inherited by autosomal recessive trait.
Step-by-step explanation:
The anemia described by the genetic defect in the beta chain of Hb inherited by autosomal recessive trait is thalassemia. Thalassemia occurs when there is a decreased rate of synthesis of one of the polypeptide chains of the globin molecule. This leads to a deficiency of the beta chain, causing the alpha chains to either combine with themselves or with other chains, resulting in low levels of Hb and impaired transport of oxygen.