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Beta-Ureidopropionase Deficiency MeSH Supplementary Concept Data 2022


MeSH Supplementary
Beta-Ureidopropionase Deficiency
Unique ID
C563210
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C563210
Registry Number
0
Heading Mapped to
*Abnormalities, Multiple
Amidohydrolases / *deficiency
*Brain Diseases
*Movement Disorders
*Purine-Pyrimidine Metabolism, Inborn Errors
Frequency
8
Note
mutation in UPB1
Date of Entry
2012/11/05
Revision Date
2013/11/06
Beta-Ureidopropionase Deficiency Preferred
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