Elliptocytosis 2

MONDO:0007533

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

9 clinical trials for this condition and its sub-types, 0 tagged with Elliptocytosis 2 itself.

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Part of

↑ Familial hemolytic anemia (27) ↑ Hereditary elliptocytosis (2)

Including sub-types (9) Tagged with Elliptocytosis 2 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.