Human genes for D-glyceric aciduria
D-glyceric aciduria [DOID:0111626]
An inherited metabolic disorder characterized by impaired serine and fructose metabolism resulting in elevated excretion of D-glyceric acid that has_material_basis_in homozygous or compound heterozygous mutation in GLYCTK on chromosome 3p21.2.
Synonyms: D-glyceric aciduria, Dglyceric aciduria, D-glyceric acidurias, DOID:0111626, deficiency of glycerate kinase ...