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Hereditary spherocytosis type 5
rareAny hereditary spherocytosis in which the cause of the disease is a mutation in the EPB42 gene.
- Identifiers
- MONDO:0012985 OMIM:612690
- Causal genes
- EPB42
- Part of
- Hereditary spherocytosis
- Also known as
- EPB42 hereditary spherocytosis · hereditary spherocytosis caused by mutation in EPB42 · HS5 · SPH5 · spherocytosis, type 5
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