C0268164 - Recessively inherited primary hyperoxaluria due to alanine-glyoxylate aminotransferase (AGXT) deficiency. 1/10
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Terms, descriptions
CUI    C0268164
NCI National Institute of Child Health and Human Development A25775364 AT210373661 Recessively inherited primary hyperoxaluria due to alanine-glyoxylate aminotransferase (AGXT) deficiency.
NCI Thesaurus A25775364 AT230074388 Recessively inherited primary hyperoxaluria due to alanine-glyoxylate aminotransferase (AGXT) deficiency.