C128804Level 6
D-Glyceric Aciduria
**Semantic type:** Disease or Syndrome
**Definition:** An autosomal recessive genetic disorder caused by mutations in the GLYCTK gene, encoding glycerate kinase. The condition is characterized by excretion of D-glyceric acid in the urine. The phenotype varies from mild to severe, and may result in encephalopathy, mental retardation, microcephaly and early death.
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