MeSH Browser

MeSH Supplementary: Methionine Malabsorption Syndrome
Unique ID: C562682
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562682
Entry Term(s): Oasthouse Urine Disease; Smith-Strang Disease
Registry Numbers: 0
Heading Mapped to: *Amino Acid Metabolism, Inborn Errors; *Intellectual Disability; Methionine; *Respiration Disorders; *Seizures
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Methionine Malabsorption Syndrome MeSH Supplementary Concept Data 2025