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Disease Ontology Browser
hereditary spherocytosis type 4 (DOID:0110919)
Alliance: disease page
Synonyms: hereditary spherocytosis 4; HS4; SPH4
Alt IDs: OMIM:612653
Definition: A hereditary spherocytosis that has_material_basis_in an autosomal dominant mutation of SLC4A1 on chromosome 17q21.31.

Disease References using Mouse Models (1)

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 6.14
The Jackson Laboratory