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Hereditary spherocytosis type 2
rareAny hereditary spherocytosis in which the cause of the disease is a mutation in the SPTB gene.
- Identifiers
- MONDO:0000913 OMIM:616649
- Causal genes
- SPTB
- Part of
- Hereditary spherocytosis
- Also known as
- hereditary spherocytosis caused by mutation in SPTB · HS2 · SPH2 · spherocytosis, type 2 · SPTB hereditary spherocytosis
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