MeSH Browser

MeSH Supplementary: Sudden Infant Death with Dysgenesis of the Testes Syndrome
Unique ID: C563856
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563856
Registry Numbers: 0
Heading Mapped to: *Sudden Infant Death; Testis / abnormalities
Frequency: 2
Note: mutation in TSPYL1
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Sudden Infant Death with Dysgenesis of the Testes Syndrome MeSH Supplementary Concept Data 2025