Osteogenesis imperfecta, Levin type [Supplementary Concept]
Date introduced: August 25, 2010
MeSH Unique ID: C536039
Heading Mapped to:
Entry Terms:
- Levin syndrome 2
- Osteogenesis imperfecta with unusual skeletal lesions
- Gnathodiaphyseal Dysplasia
- Gnathodiaphyseal Sclerosis