MeSH Browser

MeSH Supplementary: Larsen syndrome, dominant type
Unique ID: C537873
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537873
Entry Term(s): Larsen Syndrome, Autosomal Dominant
Registry Numbers: 0
Heading Mapped to: *Cleft Lip; *Cleft Palate; Joint Dislocations / congenital; *Osteochondrodysplasias; *Tooth Abnormalities; *Craniofacial Abnormalities
Frequency: 4
Note: Bilateral dislocation of the knees, pes cavus, cylindrically shaped fingers, and characteristic facies
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Larsen syndrome, dominant type MeSH Supplementary Concept Data 2025