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
00126 SCKL Seckel syndrome (SCKL) 210600 - - - ATR, CENPJ, CEP152, CEP63, NIN, RBBP8 - -
00711 SCKL-7 Seckel syndrome, type 7 (SCKL-7) 614851 - - - NIN - -
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