Orotic aciduria

MONDO:0009797

An extremely rare autosomal recessive inherited disorder caused by mutations in the UMPS gene. It is characterized by deficiency of the activity of the pyrimidine pathway enzyme uridine 5'-monophosphate (UMP) synthase. Clinical manifestations include growth retardation, anemia, and increased excretion of orotic acid in the urine.

Also known as: Hereditary Orotic Aciduria, orotic aciduria, oroticaciduria, orotidylic decarboxylase deficiency, uridine monophosphate synthetase deficiency, OPRT and ODC deficiency, UMP synthtase deficiency, UMPS

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