Beta-Ureidopropionase Deficiency MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Beta-Ureidopropionase Deficiency
Unique ID: C563210
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563210
Registry Numbers: 0
Heading Mapped to: *Abnormalities, Multiple; Amidohydrolases / deficiency; *Brain Diseases; *Movement Disorders; *Purine-Pyrimidine Metabolism, Inborn Errors
Frequency: 10
Note: mutation in UPB1
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Beta-Ureidopropionase Deficiency Preferred

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