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Hereditary spherocytosis type 2

MONDO:0000913

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

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

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