MeSH Browser

MeSH Supplementary: Pierre Robin sequence with pectus excavatum and rib and scapular anomalies
Unique ID: C535775
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535775
Entry Term(s): Campomelic dysplasia, mild
Registry Numbers: 0
Heading Mapped to: *Pierre Robin Syndrome; *Campomelic Dysplasia
Frequency: 1
Note: Skeletal dysplasia related to campomelic dysplasia
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Pierre Robin sequence with pectus excavatum and rib and scapular anomalies MeSH Supplementary Concept Data 2025