MeSH Browser

MeSH Supplementary: Maroteaux Fonfria syndrome
Unique ID: C536023
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536023
Entry Term(s): Apert syndrome with polydactyly of hands and feet; Apparent Apert syndrome with polydactyly
Registry Numbers: 0
Heading Mapped to: *Acrocephalosyndactylia; *Polydactyly
Frequency: 3
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Maroteaux Fonfria syndrome MeSH Supplementary Concept Data 2025