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Orotic Aciduria

1. UMP synthase deficiency (hereditary orotic aciduria)

2. Urea cycle defects-ornithine transcarbamylase deficiency, citrullinemia, arginosuccinic aciduria. arginemia

3. Purine nucleoside phosphorylase (PNP) deficiency

4. Phosphoribosylpyrophosphate (PRPP) synthetase deficiency

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