Hereditary spherocytosis type 3

MONDO:0010053

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

9 clinical trials for this condition and its sub-types, 0 tagged with Hereditary spherocytosis type 3 itself.

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↑ Hereditary spherocytosis (2)

Including sub-types (9) Tagged with Hereditary spherocytosis type 3 (0)

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