hypofibrinogenemia, congenital Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/202400
Similar Terms
Downloads & Tools

Genes

2 genes associated with the hypofibrinogenemia, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
FGB fibrinogen beta chain
FGG fibrinogen gamma chain