MeSH Browser

MeSH Supplementary: Pierre Robin syndrome with fetal chondrodysplasia
Unique ID: C535776
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535776
Entry Term(s): Heterozygous Osmed; Heterozygous Otospondylomegaepiphyseal Dysplasia; Weissenbacher-Zweymuller syndrome; Weissenbacher-Zweymüller Syndrome
Registry Number: 0
Heading Mapped to: *Osteochondrodysplasias; *Pierre Robin Syndrome
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2013/10/24

Pierre Robin syndrome with fetal chondrodysplasia MeSH Supplementary Concept Data 2024