MeSH Browser

MeSH Supplementary: Osteogenesis imperfecta, Levin type
Unique ID: C536039
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536039
Entry Term(s): Gnathodiaphyseal Dysplasia; Gnathodiaphyseal Sclerosis; Levin syndrome 2; Osteogenesis imperfecta with unusual skeletal lesions
Registry Number: 0
Heading Mapped to: *Osteogenesis Imperfecta
Frequency: 23
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Osteogenesis imperfecta, Levin type MeSH Supplementary Concept Data 2023