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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 LFNG 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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last database update
06/28/2022
MGI 6.20
The Jackson Laboratory