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Disease Ontology Browser
hereditary spherocytosis type 1 (DOID:0110916)
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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
08/08/2017
MGI 6.10
The Jackson Laboratory