MeSH Browser

MeSH Supplementary: Worth syndrome
Unique ID: C536748
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536748
Entry Term(s): Benign hyperostosis corticalis generalisata; Endosteal Hyperostosis, Autosomal Dominant; Endosteal hyperostosis Worth type; Hyperostosis Corticalis Generalisata, Benign Form Of Worth, With Torus Palatinus; Hyperostosis corticalis generalisata congenita; Osteosclerosis, Autosomal Dominant; Osteosclerosis, autosomal dominant Worth type with torus palatinus
Heading Mapped to: *Hyperostosis, Cortical, Congenital; *Osteopetrosis
Frequency: 5
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Worth syndrome MeSH Supplementary Concept Data 2024