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Disease Ontology Browser
spondylocostal dysostosis 2 (DOID:0112362)
Alliance: disease page
Synonyms: autosomal recessive spondylocostal dysostosis 2; SCDO2
Alt IDs: OMIM:608681
Definition: A spondylocostal dysostosis that has_material_basis_in homozygous or compound heterozygous mutation in the MESP2 gene on chromosome 15q26.1.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory