Anemia, Cooley

Anemia, Cooley's

Anemia, Cooleys

Anemia, Erythroblastic

Anemia, Mediterranean

Anemias, Erythroblastic

Anemias, Mediterranean

Cooley's Anemia

Disease, Hemoglobin F

Erythroblastic Anemia

Hemoglobin F Disease

Intermedia, Thalassemia

Intermedias, Thalassemia

Major, Thalassemia (beta-Thalassemia Major)

Majors, Thalassemia (beta-Thalassemia Major)

Mediterranean Anemia

Mediterranean Anemias

Microcytemia, beta Type

Microcytemias, beta Type

Minor, Thalassemia (beta-Thalassemia Minor)

Minors, Thalassemia (beta-Thalassemia Minor)

Thalassemia Intermedia

Thalassemia Intermedias

Thalassemia Major

Thalassemia Major (beta Thalassemia Major)

Thalassemia Major (beta-Thalassemia Major)

Thalassemia Majors (beta-Thalassemia Major)

Thalassemia Minor

Thalassemia Minor (beta Thalassemia Minor)

Thalassemia Minor (beta-Thalassemia Minor)

Thalassemia Minors (beta-Thalassemia Minor)

Thalassemia, beta

Thalassemia, beta Type

Thalassemias, beta

Thalassemias, beta Type

Type Microcytemia, beta

Type Microcytemias, beta

Type Thalassemia, beta

Type Thalassemias, beta

beta Thalassemia

beta Thalassemias

beta Type Microcytemia

beta Type Microcytemias

beta Type Thalassemia

beta Type Thalassemias

A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent.