Agent Commons Collaborative Research
Elliptocytosis 2
rareAny hereditary elliptocytosis in which the cause of the disease is a mutation in the SPTA1 gene.
- Identifiers
- MONDO:0007533 OMIM:130600
- Causal genes
- SPTA1
- Also known as
- EL2 · elliptocytosis type 2 · elliptocytosis-2 · hereditary elliptocytosis caused by mutation in SPTA1 · SPTA1 hereditary elliptocytosis
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