DO_rare_slim has material basis in autosomal recessive disease glutathione synthetase deficiency congenital nonspherocytic hemolytic anemia 6 disease_ontology DOID:0112252 MIM:231900 A congenital nonspherocytic hemolytic anemia a mild form of 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. ORDO:289849 glutathione synthetase deficiency of erythrocytes glutathione synthetase deficiency without 5-oxoprolinuria congenital nonspherocytic hemolytic anemia autosomal recessive inheritance