MeSH Browser

MeSH Supplementary: Shprintzen omphalocele syndrome
Unique ID: C537329
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537329
Entry Term(s): Laryngeal and pharyngeal hypoplasia with omphalocele; Pharynx and larynx hypoplasia with omphalocele; Shprintzen-Goldberg omphalocele syndrome
Registry Numbers: 0
Heading Mapped to: *Abnormalities, Multiple; *Hernia, Umbilical; Larynx; Pharynx; *Scoliosis; *Facies
Frequency: 0
Note: Omphalocele with hypoplasia of pharynx and larynx, learning disability, dysmorphic facies, and scoliosis; Omphalocele with hypoplasia of pharynx and larynx, learning disability, dysmorphic facies, and scoliosis
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Shprintzen omphalocele syndrome MeSH Supplementary Concept Data 2025