MeSH Browser

MeSH Supplementary: Camptodactyly taurinuria
Unique ID: C537972
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537972
Entry Term(s): Camptodactyly with Taurinuria
Registry Numbers: 0
Heading Mapped to: *Amino Acid Metabolism, Inborn Errors; *Hand Deformities, Congenital; Taurine / urine
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Camptodactyly taurinuria MeSH Supplementary Concept Data 2025