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Up to: Hereditary disease · Hemoglobinopathy
Inherited hemoglobinopathy
An inherited disorder characterized by structural alterations of a globin chain within the hemoglobin molecule.
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Sickle cell disease 342 trials Sub-types →
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Thalassemia 49 trials · 129 incl. sub-types Sub-types →
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Beta-thalassemia and related diseases 0 trials · 99 incl. sub-types Sub-types →
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Congenital nonspherocytic hemolytic anemia 1 trial · 12 incl. sub-types Sub-types →
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Sickle cell-beta-thalassemia disease syndrome 5 trials · 9 incl. sub-types Sub-types →
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Hemoglobin C disease 2 trials
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Unstable hemoglobin disease 1 trial
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Hereditary methemoglobinemia 0 trials · 1 incl. sub-types Sub-types →
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Hemoglobin D disease 0 trials
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Hemoglobin E disease 0 trials
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Hemoglobinopathy Toms River 0 trials
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Homozygous hemoglobin O Arab disease 0 trials
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Sulfhemoglobinemia, congenital 0 trials