factor VIII deficiency

Summary
Synonym
  • Congenital factor VIII disorder
  • Hemophilia A
  • Subhemophilia
  • classic hemophilia A
Definition
A blood coagulation disease that has_material_basis_in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged.
Super Class
X-linked recessive disease blood coagulation disease
Disease Ontology
DOID:12134
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 1 - 10 of 13 in total
Gene ID Gene Symbol Description Source
629 CFB complement factor B
718 C3 complement C3
727 C5 complement C5
2147 F2 coagulation factor II, thrombin
2157 F8 coagulation factor VIII
2212 FCGR2A Fc gamma receptor IIa
3117 HLA-DQA1 major histocompatibility complex, class II, DQ alpha 1
3458 IFNG interferon gamma
3586 IL10 interleukin 10
5199 CFP complement factor properdin
Displaying entries 11 - 14 of 14 in total
Gene ID Gene Symbol Description Source
18636 Cfp complement factor properdin
18791 Plat plasminogen activator, tissue
21788 Tfpi tissue factor pathway inhibitor
21803 Tgfb1 transforming growth factor, beta 1
Displaying all 9 entries
Gene ID Gene Symbol Description Source
24232 C3 complement C3
25325 Il10 interleukin 10
25692 Plat plasminogen activator, tissue type
25712 Ifng interferon gamma
29436 Tfpi tissue factor pathway inhibitor
59086 Tgfb1 transforming growth factor, beta 1
116591 Fcgr2a Fc gamma receptor 2A
289211 Fcgr2b Fc gamma receptor 2B
498276 Fcgr2al1 Fc gamma receptor 2A like 1
Displaying 1 entry
Gene ID Gene Symbol Description Source Organism
397778 tgfb1.L transforming growth factor beta 1 L homeolog Xenopus laevis (African clawed frog)

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Acknowledgements

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Last updated: December 9, 2024