MeSH Browser

MeSH Supplementary: Tryptophanuria With Dwarfism
Unique ID: C562658
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562658
Registry Numbers: 0
Heading Mapped to: *Amino Acid Metabolism, Inborn Errors; *Ataxia; *Dwarfism; *Intellectual Disability
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Tryptophanuria With Dwarfism MeSH Supplementary Concept Data 2025