MeSH Browser

MeSH Supplementary: Osteopetrosis autosomal dominant type 1
Unique ID: C536056
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536056
Entry Term(s): Osteopetrosis, Autosomal Dominant 1; Osteopetrosis, Autosomal Dominant, Type I
Registry Numbers: 0
Heading Mapped to: Osteopetrosis / congenital
Frequency: 3
Note: mutationin LRP5
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Osteopetrosis autosomal dominant type 1 MeSH Supplementary Concept Data 2025