MeSH Browser

MeSH Supplementary: Phenol sulfotransferase deficiency
Unique ID: C537895
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537895
Registry Numbers: 0
Heading Mapped to: *Metabolism, Inborn Errors; Arylsulfotransferase / deficiency
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Phenol sulfotransferase deficiency MeSH Supplementary Concept Data 2025