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Disease Ontology Browser
hereditary spherocytosis type 1 (DOID:0110916)
Alliance: disease page
Synonyms: hereditary spherocytosis 1; HS1; SPH1
Alt IDs: OMIM:182900
Definition: A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of ANK1 on chromosome 8p11.21.

Disease References using Mouse Models (11)

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
MGI 6.19
The Jackson Laboratory