All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03220 POF7 ovarian failure, premature, type 7 (POF-7) 612964 AD - - NR5A1 - -
03496 SPGF8 spermatogenic failure, type 8 (SPGF-8) 613957 AD - - NR5A1 - -
05584 SRXX4 46,XX sex reversal, type 4 (SRXX-4) 617480 AD - - NR5A1 - autosomal dominant
03221 SRXY3 46,XY sex reversal, type 3 (SRXY-3) 612965 AD 16 16 NR5A1 - -
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