abnormality of circulating fibrinogen Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the level of activity of circulating fibrinogen. (Human Phenotype Ontology, HP_0011898)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011898
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Genes

7 genes associated with the abnormality of circulating fibrinogen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FGA fibrinogen alpha chain
FGB fibrinogen beta chain
FGG fibrinogen gamma chain
PRF1 perforin 1 (pore forming protein)
STX11 syntaxin 11
UNC13D unc-13 homolog D (C. elegans)
XIAP X-linked inhibitor of apoptosis, E3 ubiquitin protein ligase