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
03288 F13AD deficiency, factor XIII (A subunit) (F13AD) 613225 AR 1 1 F13A1 - -
02760 MCI1 myocardial infarction, susceptibility to, type 1 (MCI-1) 608446 - 41 2 ESR1, F13A1, F7, GCLC, GCLM, ITGB3, LGALS2, LTA, MIAT, OLR1, PSMA6, TNFSF4 - -
01581 THPH1 thrombophilia,due to thrombin defect (THPH1) 188050 AD 4 4 F13A1, F2, HABP2, MTHFR - -
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