MeSH Browser

MeSH Supplementary: Xanthinuria, Type II
Unique ID: C566358
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566358
Entry Term(s): Xanthine Dehydrogenase and Aldehyde Oxidase, Combined Deficiency of
Registry Number: 0
Heading Mapped to: *Purine-Pyrimidine Metabolism, Inborn Errors; Xanthine Dehydrogenase / *deficiency; Xanthine; Aldehyde Oxidase / *deficiency
Frequency: 6
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Xanthinuria, Type II MeSH Supplementary Concept Data 2024