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Standards Ontologies Notations
osteogenesis imperfecta type 9

Summary
Synonym
  • OI9
  • osteogenesis imperfecta type IX
Definition
An osteogenesis imperfecta that has_material_basis_in mutation in the PPIB gene on chromosome 15q22.
Super Class
autosomal recessive disease osteogenesis imperfecta
Disease Ontology
DOID:0110349
Mondo Disease Ontology
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
5479 PPIB peptidylprolyl isomerase B
Displaying 1 entry
Gene ID Gene Symbol Description Source
19035 Ppib peptidylprolyl isomerase B
Displaying 1 entry
Gene ID Gene Symbol Description Source
175231 cyn-6 Peptidyl-prolyl cis-trans isomerase 6
Displaying 1 entry
Gene ID Gene Symbol Description Source
851898 CPR5 peptidylprolyl isomerase family protein CPR5
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024