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
03485 CFDD deficiency, complement factor D (CFDD) 613912 AR - - CFD - -
03372 F5F8D2 deficiency, combined, factor V and factor VIII, type 2 (F5F8D-2) 613625 - - - MCFD2 - -
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