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
06740 FANCU ?Fanconi anemia, complementation group U 617247 AR - - XRCC2 - -
05186 POF17 ovarian failure, premature, type 17 619146 AR - - XRCC2 - -
06908 SPGF50 spermatogenic failure, type 50 619145 AR - - XRCC2 - -
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