All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00201 INFM infertility, male (INFM) - - 173 141 ACTL9, AURKC, CXorf59, DPY19L2, M1AP, MAATS1, MNS1, MSH4, MSH5 - -
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