Agent Commons Collaborative Research
Beta-ureidopropionase deficiency
rareBeta-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).
- Identifiers
- MONDO:0013164 OMIM:613161Orphanet:65287
- Causal genes
- UPB1
- Also known as
- Beta-alanine synthase deficiency · UPB1D
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