factor V deficiency

Summary
Synonym
  • Hereditary hypoproaccelerinaemia
  • Labile factor deficiency
  • Proaccelerin deficiency
  • deficiency, labile
Super Class
autosomal recessive disease blood coagulation disease
Disease Ontology
DOID:2216
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
Related Genes
Displaying all 3 entries
Gene ID Gene Symbol Description Source
2153 F5 coagulation factor V
3998 LMAN1 lectin, mannose binding 1
7035 TFPI tissue factor pathway inhibitor
Displaying all 3 entries
Gene ID Gene Symbol Description Source
14067 F5 coagulation factor V
21788 Tfpi tissue factor pathway inhibitor
70361 Lman1 lectin, mannose-binding, 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
29436 Tfpi tissue factor pathway inhibitor

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024