MeSH Browser

MeSH Supplementary: Opitz Reynolds Fitzgerald syndrome
Unique ID: C535713
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535713
Registry Numbers: 0
Heading Mapped to: *Facial Asymmetry; *Mandibulofacial Dysostosis
Frequency: 0
Note: Bilateral hemifacial microsomia with hearing loss, telecanthus, tetramelic postaxial hexadactyly, congenital hypotonia and lymphedema with joint hypermobility, and pigmentary dysplasia
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Opitz Reynolds Fitzgerald syndrome MeSH Supplementary Concept Data 2025