All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00200 SPGFY2 spermatogenic failure, Y-linked, type 2 (SPGFY-2) 415000 YL 1 1 USP9Y - -
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