All diseases

OMIM ID
202400
OMIM term:
AFIBRINOGENEMIA, CONGENITAL HYPOFIBRINOGENEMIA, CONGENITAL, INCLUDED
Alternative terms:
DYSFIBRINOGENEMIA, CONGENITAL, INCLUDED
HYPODYSFIBRINOGENEMIA, CONGENITAL, INCLUDED
(∗) Location:
4q31.3  
(†) Associated OMIM genes:
FGA   FGB  
(‡) Associated MGI genes:
Fgg  

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* quick link - http://q.sanger.ac.uk/o7sefhi9