Elliptocytosis 2

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

Also known as: SPTA1 hereditary elliptocytosis, elliptocytosis 2, elliptocytosis type 2, elliptocytosis-2, hereditary elliptocytosis caused by mutation in SPTA1, EL2, elliptocytosis, Rhesus-unlinked type

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