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
06066 HYDNP1 Hydrocephalus, normal pressure, 1 236690 AD - - WDR96 - -
05567 SPGF19 spermatogenic failure, type 19 (SPGF-19) 617592 AR - - WDR96 - autosomal recessive
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