Hereditary spherocytosis type 3

Any hereditary spherocytosis in which the cause of the disease is a mutation in the SPTA1 gene.

Also known as: HS3, SPH3, SPTA1 hereditary spherocytosis, hereditary spherocytosis caused by mutation in SPTA1, spherocytosis, hereditary, 3, spherocytosis, type 3

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