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DOID:0112365 - spondylocostal dysostosis 1
Disease Ontology Definition:A spondylocostal dysostosis that has_material_basis_in homozygous or compound heterozygous mutation in the DLL3 gene on chromosome 19q13.2.
Synonyms: SCDO1, autosomal recessive spondylocostal dysostosis 1,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MIM:277300 - spondylocostal dysostosis 1, autosomal recessive; scdo1 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee