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Ontology Browser

Term:
osteogenesis imperfecta type 16 (DOID:0110345)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Al Gazali Sabrinathan Nair Syndrome 
Astley-Kendall Syndrome 
Bruck syndrome +   
Cole-Carpenter syndrome +   
gnathodiaphyseal dysplasia  
Grant Syndrome 
Lowry Maclean syndrome 
OI/EDS Combined Syndrome  
Osteogenesis Imperfecta Congenita, Microcephaly, and Cataracts 
osteogenesis imperfecta type 1  
osteogenesis imperfecta type 10  
osteogenesis imperfecta type 11  
osteogenesis imperfecta type 12  
osteogenesis imperfecta type 13  
osteogenesis imperfecta type 14  
osteogenesis imperfecta type 15  
osteogenesis imperfecta type 16  
An osteogenesis imperfecta that has_material_basis_in contiguous gene deletion on chromosome 11p11. (DO)
osteogenesis imperfecta type 17  
osteogenesis imperfecta type 18  
osteogenesis imperfecta type 19  
osteogenesis imperfecta type 2 +   
osteogenesis imperfecta type 20  
osteogenesis imperfecta type 3  
osteogenesis imperfecta type 4  
osteogenesis imperfecta type 5  
osteogenesis imperfecta type 6  
osteogenesis imperfecta type 7  
osteogenesis imperfecta type 8  
osteogenesis imperfecta type 9  
osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures 
Osteopenic Nonfracture Syndrome 
osteoporosis-pseudoglioma syndrome  

Synonyms
Exact Synonyms: OI16 ;   chromosome 11p11.2 deletion syndrome 91.3-KB ;   osteogenesis imperfecta type XVI
Primary IDs: OMIM:616229
Alternate IDs: RDO:9002967
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/24079343 "DO"

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.