Adenine phosphoribosyltransferase deficiency

MONDO:0013869

Adenine phosphoribosyltransferase (APRT) deficiency is a rare autosomal recessive (AR) disorder characterized by the formation and hyperexcretion of 2,8-dihydroxyadenine (2,8-DHA) in urine, causing urolithiasis and crystalline nephropathy.

Also known as: 2,8-dihydroxyadenine urolithiasis, 2,8-dihydroxyadeninuria disease, APRT deficiency, adenine phosphoribosyltransferase deficiency, APRTD, Dihydroxyadeninuria, nephrolithiasis, Dha, urolithiasis, 2,8-dihydroxyadenine

27 clinical trials for this condition and its sub-types.

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