MeSH Browser

MeSH Supplementary: Osteogenesis imperfecta, type 3
Unique ID: C536044
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536044
Entry Term(s): OI, type 3 Osteogenesis imperfecta, type 3; OI, type III Osteogenesis imperfecta, type III; OI3 Osteogenesis imperfecta 3; Osteogenesis Imperfecta, Type III; Osteogenesis imperfecta, progressively deforming, with normal sclerae
Heading Mapped to: *Osteogenesis Imperfecta
Frequency: 48
Note: An autosomal dominant form of osteogenesis imperfecta caused by mutations in the COL1A1 or COL1A2 genes. OMIM: 259420
Date of Entry: 2010/08/25
Revision Date: 2019/06/20

Osteogenesis imperfecta, type 3 MeSH Supplementary Concept Data 2024