MeSH Browser

MeSH Supplementary: Kenny-Caffey syndrome, Type 1
Unique ID: C537021
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537021
Entry Term(s): Kenny Caffey syndrome; Kenny syndrome; Kenny-Caffey Syndrome, Autosomal Recessive; Kenny-Caffey syndrome, autosomal recessive form
Registry Numbers: 0
Heading Mapped to: *Hyperostosis, Cortical, Congenital
Frequency: 2
Date of Entry: 2010/08/25
Revision Date: 2018/09/24

Kenny-Caffey syndrome, Type 1 MeSH Supplementary Concept Data 2025