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Disease Ontology Browser
glutathione synthetase deficiency of erythrocytes (DOID:0112252)
Alliance: disease page
Synonyms: glutathione synthetase deficiency without 5-oxoprolinuria
Alt IDs: OMIM:231900, ORDO:289849
Definition: A glutathione synthetase deficiency characterized by hemolytic anemia and deficiency in GSH that is limited to the red blood cells, with nucleated cells able to maintain normal or near normal expression levels that has_material_basis_in homozygous or compound heterozygous mutation in GSS on chromosome 20q11.22.

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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory