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Hereditary spherocytosis type 3
rareAny hereditary spherocytosis in which the cause of the disease is a mutation in the SPTA1 gene.
- Identifiers
- MONDO:0010053 OMIM:270970
- Causal genes
- SPTA1
- Part of
- Hereditary spherocytosis
- Also known as
- hereditary spherocytosis caused by mutation in SPTA1 · HS3 · SPH3 · spherocytosis, type 3 · SPTA1 hereditary spherocytosis
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