Factor VII deficiency

Disease ID:342
Name:Factor VII deficiency
Associated with:2 targets
0 immuno-relevant targets
0 immuno-relevant ligands
Database Links
Disease Ontology: DOID:2215
OMIM: 227500
Orphanet: ORPHA327


Hepatocyte nuclear factor-4-α
Role:  Mutations in the HNF4 alpha binding site in the blood coagulation Factor VII gene result in this inherited bleeding disorder.
References:  1


No ligand related data available for Factor VII deficiency


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1. Arbini AA, Pollak ES, Bayleran JK, High KA, Bauer KA. (1997) Severe factor VII deficiency due to a mutation disrupting a hepatocyte nuclear factor 4 binding site in the factor VII promoter. Blood, 89 (1): 176-82. [PMID:8978290]