MeSH Browser

MeSH Supplementary: Gay Feinmesser Cohen syndrome
Unique ID: C537676
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537676
Entry Term(s): Laryngeal web, congenital heart disease and low stature; Subglottic bar, congenital heart disease and low stature
Registry Number: 0
Heading Mapped to: Glottis / *abnormalities; *Growth Disorders; *Heart Defects, Congenital
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Gay Feinmesser Cohen syndrome MeSH Supplementary Concept Data 2023