MeSH Browser

MeSH Supplementary: Catel Manzke syndrome
Unique ID: C535347
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535347
Entry Term(s): Catel-Manzke Syndrome; Hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome; Index Finger Anomaly With Pierre Robin Syndrome; Palatodigital syndrome, Catel-Manzke type; Pierre Robin syndrome with hyperphalangy and clinodactyly
Registry Numbers: 0
Heading Mapped to: *Hand Deformities, Congenital; *Pierre Robin Syndrome
Frequency: 12
Date of Entry: 2010/08/25
Revision Date: 2012/08/24

Catel Manzke syndrome MeSH Supplementary Concept Data 2025