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Disease Ontology Browser
spondylocostal dysostosis 3 (DOID:0112361)
Alliance: disease page
Synonyms: autosomal recessive spondylocostal dysostosis 3; SCDO3
Alt IDs: OMIM:609813
Definition: A spondylocostal dysostosis that has_material_basis_in homozygous or compound heterozygous mutation in the LFNG gene on chromosome 7p22.3.

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
12/17/2024
MGI 6.24 		The Jackson Laboratory