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Disease Ontology Browser
hereditary spherocytosis type 3 (DOID:0110918)
Alliance: disease page
Synonyms: hereditary spherocytosis 3; HS3; SPH3
Alt IDs: OMIM:270970
Definition: A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of SPTA1 on chromosome 1q23.1.

Disease References using Mouse Models (7)

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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last database update
11/10/2020
MGI 6.16
The Jackson Laboratory