Hereditary spherocytosis type 5

MONDO:0012985

Any hereditary spherocytosis in which the cause of the disease is a mutation in the EPB42 gene.

Also known as: EPB42 hereditary spherocytosis, HS5, SPH5, hereditary spherocytosis caused by mutation in EPB42, hereditary spherocytosis type 5, spherocytosis, hereditary, 5, spherocytosis, type 5

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