All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02118 SCDO1 dysostosis, spondylocostal, autosomal recessive, type 1 (SCDO-1, Jarcho-Levin syndrome) 277300 AR - - DLL3, MESP2 - -
02781 SCDO2 dysostosis, spondylocostal, autosomal recessive, type 2 (SCDO-2) 608681 AR - - MESP2 - -
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