MeSH Browser

MeSH Supplementary: Lysine Malabsorption Syndrome
Unique ID: C563080
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563080
Registry Numbers: 0
Heading Mapped to: *Amino Acid Metabolism, Inborn Errors; Lysine / metabolism; *Malabsorption Syndromes
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Lysine Malabsorption Syndrome MeSH Supplementary Concept Data 2025