Hereditary spherocytosis type 2

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

Also known as: HS2, SPH2, SPTB hereditary spherocytosis, hereditary spherocytosis caused by mutation in SPTB, hereditary spherocytosis type 2, spherocytosis, type 2, spherocytosis, hereditary, 2

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