Orotic Aciduria

Alternative Names

  • Orotic Aciduria I
  • Orotate Phosphoribosyltransferase and Orotidylic Decarboxylase Deficiency
  • OPRT and ODC Deficiency
  • Orotidylic Pyrophosphorylase and Orotidylic Decarboxylase Deficiency
  • Uridine Monophosphate Synthase Deficiency
  • UMP Synthase Deficiency
  • UMPS Deficiency
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WHO-ICD-10 version:2010

Congenital malformations, deformations and chromosomal abnormalities

Congenital malformations and deformations of the musculoskeletal system

OMIM Number

258900

Mode of Inheritance

Autosomal recessive

Gene Map Locus

3q21.2

Description

Orotic aciduria is a rare autosomal recessive disorder characterized by megaloblastic anemia and orotic acid crystalluria that is frequently associated with some degree of physical and mental retardation. These features respond to appropriate pyrimidine replacement therapy, and most cases appear to have a good prognosis. A minority of cases have additional features, particularly congenital malformations and immune deficiencies, which may adversely affect this prognosis. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
258900.1.1United Arab EmiratesFemaleYes Very preterm birth; Failure to thrive; R...NM_000373.4:c.1010C>GHomozygousAutosomal, RecessiveAl Absi et al. 2021 Proband
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