Beta-ureidopropionase deficiency

MONDO:0013164

Beta-ureidopropionase deficiency is a very rare pyrimidine metabolism disorder described in fewer than 10 patients to date with an extremely wide clinical picture ranging from asymptomatic cases to neurological (epilepsy, autism) and developmental disorders (urogenital, colorectal).

Also known as: Beta-alanine synthase deficiency, beta-ureidopropionase deficiency, BETA-ureidopropionase deficiency, UPB1D

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

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