MeSH Browser

MeSH Supplementary: TARP syndrome
Unique ID: C536942
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536942
Entry Term(s): Pierre Robin syndrome with congenital heart malformation and clubfoot; Talipes Equinovarus, Atrial Septal Defect, Robin Sequence, and Persistence of Left Superior Vena Cava
Registry Number: 0
Heading Mapped to: *Clubfoot; *Heart Defects, Congenital; *Pierre Robin Syndrome
Frequency: 15
Note: TARPS=Talipes equinovarus, atrial septal defect, robin sequence, and persistence of left superior vena cava
Date of Entry: 2010/08/25
Revision Date: 2012/08/24

TARP syndrome MeSH Supplementary Concept Data 2023