Hereditary spherocytosis type 5
MONDO:0012985Any 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
9 clinical trials for this condition and its sub-types, 0 tagged with Hereditary spherocytosis type 5 itself.
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