MeSH Browser

MeSH Supplementary: Cystathionase Deficiency
Unique ID: C562680
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562680
Registry Numbers: 0
Heading Mapped to: *Amino Acid Metabolism, Inborn Errors; Cystathionine gamma-Lyase / deficiency
Frequency: 6
Note: mutation in cystathionine gamma-lyase
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Cystathionase Deficiency MeSH Supplementary Concept Data 2025