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Standards Ontologies Notations
osteogenesis imperfecta type 10

Summary
Synonym
  • OI10
  • osteogenesis imperfecta type X
Definition
An osteogenesis imperfecta that has_material_basis_in mutation in the SERPINH gene on chromosome 11q13.
Super Class
autosomal recessive disease osteogenesis imperfecta
Disease Ontology
DOID:0110346
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
871 SERPINH1 serpin family H member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
12406 Serpinh1 serine (or cysteine) peptidase inhibitor, clade H, member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
29345 Serpinh1 serpin family H member 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