All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02251 NSX N syndrome (NSX) 310465 - - - POLA1 - -
06873 PDR Pigmentary disorder, reticulate, with systemic manifestations, X-linked 301220 XLR - - POLA1 - -
06866 VEODS Van Esch-O'Driscoll syndrome 301030 XLR - - POLA1 - -
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