Hemoglobinopathies

A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.

Year introduced: 1968

PubMed search builder options

Subheadings:

Restrict to MeSH Major Topic.

Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C15.378.420, C16.320.365

MeSH Unique ID: D006453

Entry Terms:

• Hemoglobinopathy

See Also:

• Hemoglobins, Abnormal

All MeSH Categories
Diseases Category
Hemic and Lymphatic Diseases
Hematologic Diseases
Hemoglobinopathies
Anemia, Sickle Cell
Acute Chest Syndrome
Hemoglobin SC Disease
Sickle Cell Trait
Hemoglobin C Disease
Thalassemia
alpha-Thalassemia +
beta-Thalassemia
delta-Thalassemia

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Hemoglobinopathies
Anemia, Sickle Cell
Acute Chest Syndrome
Hemoglobin SC Disease
Sickle Cell Trait
Hemoglobin C Disease
Thalassemia
alpha-Thalassemia +
beta-Thalassemia
delta-Thalassemia