Hereditary spherocytosis type 5

Any hereditary spherocytosis in which the cause of the disease is a mutation in the EPB42 gene.

Also known as: EPB42 hereditary spherocytosis, HS5, SPH5, hereditary spherocytosis caused by mutation in EPB42, hereditary spherocytosis type 5, spherocytosis, hereditary, 5, spherocytosis, type 5

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