NLM Logo

Worth syndrome MeSH Supplementary Concept Data 2024


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
Registry Number
0
Heading Mapped to
*Hyperostosis, Cortical, Congenital
*Osteopetrosis
Frequency
5
Date of Entry
2010/08/25
Revision Date
2012/11/05
Worth syndrome Preferred
page delivered in 0.005s