# hereditary spherocytosis type 4

> hereditary spherocytosis that has material basis in an autosomal dominant mutation of SLC4A1 on chromosome 17q21.31

**Wikidata**: [Q32144745](https://www.wikidata.org/wiki/Q32144745)  
**Source**: https://4ort.xyz/entity/hereditary-spherocytosis-type-4


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE).
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)