fibrochondrogenesis 2

Summary
Definition
A fibrochondrogenesis that has_material_basis_in homozygous or heterozygous mutation in the COL11A2 gene on chromosome 6p21.3.
Super Class
autosomal dominant disease autosomal recessive disease fibrochondrogenesis
Disease Ontology
DOID:0080673
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