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Digenic alpha thalassemia spectrum

MONDO:0100563

An instance of alpha thalessemia spectrum that is caused by an inherited multiallelic modification in an individual.

53 clinical trials for this condition and its sub-types.

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Sub-types

Hemoglobin H disease (5) Hb Bart's hydrops fetalis (2) HBA1; HBA2-related digenic alpha thalassemia spectrum (0)

Broader categories

Disease (618) Hereditary disease (172) Hematologic disorder (160) Thalassemia (40) Inherited hemoglobinopathy (33) Hemoglobinopathy (30) Human disease (14) Alpha thalassemia spectrum (10) Erythrocyte disorder (6) Disease of genetic or genomic mechanism (2)
Trials to join now! 22 Not yet recruiting 5 Not yet finished but already full! 8 Completed 17 Terminated 1
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