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
02419 GCLEB Gracile bone dysplasia 602361 AD - - FAM111A - -
01290 KCS2 Kenny-Caffey syndrome, type 2 127000 AD 2 2 FAM111A - -
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