MeSH Browser

MeSH Supplementary: Robinow Syndrome
Unique ID: C562492
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562492
Entry Term(s): Acral Dysostosis with Facial and Genital Abnormalities; Fetal Face Syndrome; Mesomelic Dwarfism-Small Genitalia Syndrome; Robinow Dwarfism; Robinow Syndrome, Autosomal Dominant; Robinow-Silverman-Smith Syndrome
Heading Mapped to: *Dwarfism; *Urogenital Abnormalities; *Limb Deformities, Congenital; *Craniofacial Abnormalities
Frequency: 39
Date of Entry: 2012/11/05
Revision Date: 2019/04/01

Robinow Syndrome MeSH Supplementary Concept Data 2024