NLM Logo

Osteogenesis imperfecta, type 3 MeSH Supplementary Concept Data 2024


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
Registry Number
0
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 Preferred
page delivered in 0.004s