MeSH Browser

MeSH Supplementary: Femoral facial syndrome
Unique ID: C537916
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537916
Entry Term(s): Femoral Hypoplasia-Unusual Facies Syndrome; Femoral dysgenesis, bilateral; Femoral dysgenesis, bilateral-Robin anomaly; Femoral hypoplasia unusual facies syndrome; Femoral-Facial Syndrome
Registry Numbers: 0
Heading Mapped to: Femur / abnormalities; *Pierre Robin Syndrome
Frequency: 13
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Femoral facial syndrome MeSH Supplementary Concept Data 2024