MeSH Browser

MeSH Supplementary: Grant syndrome
Unique ID: C537293
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537293
Registry Numbers: 0
Heading Mapped to: *Abnormalities, Multiple; *Osteogenesis Imperfecta; *Craniofacial Abnormalities
Frequency: 0
Note: Persistent wormian bones, blue sclerae, mandibular hypoplasia, shallow glenoid fossae and campomelia
Source: Clin Genet. 1986;29(6):523-9
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Grant syndrome MeSH Supplementary Concept Data 2025