MeSH Browser

MeSH Supplementary: Rommen Mueller Sybert syndrome
Unique ID: C535871
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535871
Entry Term(s): Developmental delay, growth deficiency, congenital heart defect, and multiple craniofacial anomalies; Short stature, heart defect and craniofacial anomalies
Registry Numbers: 0
Heading Mapped to: *Dwarfism; *Growth Disorders; *Heart Defects, Congenital; *Craniofacial Abnormalities
Frequency: 1
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Rommen Mueller Sybert syndrome MeSH Supplementary Concept Data 2025