otospondylomegaepiphyseal dysplasia, autosomal dominant

Summary
Definition
An osteochondrodysplasia that is characterized by by autosomal dominant inheritance of mutations in the COL11A2 gene.
Super Class
autosomal dominant disease osteochondrodysplasia
Disease Ontology
DOID:0080677
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
1302 COL11A2 collagen type XI alpha 2 chain
Displaying 1 entry
Gene ID Gene Symbol Description Source
12815 Col11a2 collagen, type XI, alpha 2

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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