E79.89 OTH DISRD OF PURINE AND PYRIMIDINE METABOLISM

Synonyms

• 5-amino-4-imidazole carboxamide ribosiduria
• Adenine phosphoribosyl transferase deficiency type I
• Adenine phosphoribosyl transferase deficiency type II
• Adenylosuccinate lyase deficiency
• APRT deficiency, Japanese type
• Beta-aminoisobutyric aciduria
• Congenital anomaly of macula
• Cytosine diphosphate choline phosphotransferase deficiency
• Deficiency of 3'-nucleotidase
• Deficiency of 5'-nucleotidase
• Deficiency of adenine deaminase
• Deficiency of allantoicase
• Deficiency of allantoinase
• Deficiency of AMP deaminase
• Deficiency of AMP nucleosidase
• Deficiency of AMP pyrophorylase
• Deficiency of aspartate carbamoyltransferase
• Deficiency of beta-ureidopropionase
• Deficiency of cytidine deaminase
• Deficiency of dihydrouracil dehydrogenase
• Deficiency of DNA repair
• Deficiency of glycine formiminotransferase
• Deficiency of GMP synthase
• Deficiency of homologous recombination deoxyribonucleic acid repair
• Deficiency of phosphoribosylaminoimidazole carboxylase
• Deficiency of phosphoribosylaminoimidazolecarboxamide formyltransferase
• Deficiency of phosphoribosylaminoimidazole-succinocarboxamide synthase
• Deficiency of phosphoribosylformylglycinamidine cyclo-ligase
• Deficiency of phosphoribosylformylglycinamidine synthase
• Deficiency of thymidine phosphorylase
• Deficiency of trimetaphosphatase
• Deficiency of uridine phosphorylase
• Deficiency of xanthine oxidase
• Dihydropyrimidinase deficiency
• Dihydropyrimidine dehydrogenase deficiency
• DNA repair
• DNA repair
• Hereditary orotic aciduria
• Hereditary orotic aciduria, type 1
• Hereditary orotic aciduria, type 2
• Hyperuricuria
• Hypouricemia
• Inosine triphosphate pyrophosphohydrolase deficiency
• NUDT15 deficiency
• Orotic aciduria
• Phosphoribosylpyrophosphate synthetase superactivity
• Ribose-phosphate pyrophosphokinase overactivity
• Secondary orotic aciduria
• Uridine monophosphate hydrolase deficiency

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