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Disease Ontology Browser
atypical Gaucher's disease due to saposin c deficiency (DOID:0110961)
Alliance: disease page
Alt IDs: OMIM:610539, ICD10CM:E75.2, ORDO:309252
Definition: A Gaucher's disease that has_material_basis_in an autosomal recessive mutation of PSAP on chromosome 10q22.1.

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 6.22
The Jackson Laboratory