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
02083 SMEDSL dysplasia, spondylometaepiphyseal, short limb-hand type 271665 AR - - DDR2 - -
06041 WRCN Warburg-Cinotti syndrome 618175 AD - - DDR2 - -
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