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Disease Ontology Browser
hereditary spherocytosis type 2 (DOID:0110917)
Alliance: disease page
Synonyms: hereditary spherocytosis 2; HS2; SPH2
Alt IDs: OMIM:616649
Definition: A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of the SPTB gene on chromosome 14q23.3.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
04/30/2024
MGI 6.23 		The Jackson Laboratory