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
02823 anemia anemia, aplastic, incl. susceptibility to 609135 - 46 46 IFNG, NBN, PRF1, SBDS - -
02459 FHL2 lymphohistiocytosis, hemophagocytic, familial, type 2 (FHL-2) 603553 AR 2 2 PRF1 - -
02530 lymphoma lymphoma, non-Hodgkin, familial 605027 - 9 9 BCL10, CASP10, PRF1, RAD54B, RAD54L - -
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