Search Ontology:
Human Disease
hereditary spherocytosis type 3
- Term ID
- DOID:0110918
- Synonyms
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- hereditary spherocytosis 3
- HS3
- SPH3
- Definition
- A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SPTA1 gene on chromosome 1q23.1. https://www.ncbi.nlm.nih.gov/pubmed/8941647
- References
- Ontology
- Human Disease ( DOID:0110918 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models