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Standards Ontologies Notations
osteogenesis imperfecta type 16

Summary
Synonym
  • OI16
  • chromosome 11p11.2 deletion syndrome 91.3-KB
  • osteogenesis imperfecta type XVI
Definition
An osteogenesis imperfecta that has_material_basis_in contiguous gene deletion on chromosome 11p11.
Super Class
osteogenesis imperfecta
Disease Ontology
DOID:0110345
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
90993 CREB3L1 cAMP responsive element binding protein 3 like 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
26427 Creb3l1 cAMP responsive element binding protein 3-like 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
362165 Creb3l1 cAMP responsive element binding protein 3-like 1
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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