Annotation Detail
Information
- Associated Genes
- VKORC1
- Associated Variants
-
VKORC1 MUTATION
VKORC1 MUTATION - Associated Disease
- Vitamin K Deficiency
- Source Database
- DisGeNET
- Description
- Functional limitations for the vitamin K cycle, caused either by mutations in gamma-glutamyl carboxylase or vitamin K epoxide reductase genes, result in hereditary deficiency of vitamin K-dependent coagulation factors (VKCFD1 and VKCFD2, respectively).
- Pubmed
- 25151188
- Section of the abstract supporting the evidence
- ALL_TEXT_1/3
- Number of the section of the abstract supporting the evidence
- 1
- Number of the sentence supporting the evidence
- 1
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000542883744160607
Drugs