MeSH Browser

MeSH Supplementary: Singleton Merten syndrome
Unique ID: C537343
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537343
Entry Term(s): Merten-Singleton syndrome; Singleton-Merten Syndrome
Registry Number: 0
Heading Mapped to: *Aortic Diseases; *Dental Enamel Hypoplasia; Metacarpus / *abnormalities; *Muscular Diseases; *Osteoporosis; *Odontodysplasia; *Vascular Calcification
Frequency: 31
Note: SM syndrome; "Syndrome of widened medullary cavities of the metacarpals and phalanges, aortic calcification and abnormal dentition"; and "Widened medullary cavities of bone, aortic calcification, abnormal dentition, and muscular weakness" not included
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Singleton Merten syndrome MeSH Supplementary Concept Data 2024