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Disease Ontology Browser
hereditary spherocytosis type 5 (DOID:0110920)
Alliance: disease page
Synonyms: hereditary spherocytosis 5; HS5; SPH5
Alt IDs: OMIM:612690
Definition: A hereditary spherocytosis that has_material_basis_in a mutation of EPB42 on chromosome 15q15.2.


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