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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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
External Links
- Disease Ontology
- DOID:12134
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- OMIM
- GARD
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 28 | ABO | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | |
| 2523 | FUT1 | fucosyltransferase 1 (H blood group) | |
| 2539 | G6PD | glucose-6-phosphate dehydrogenase | |
| 2990 | GUSB | glucuronidase beta | |
| 3998 | LMAN1 | lectin, mannose binding 1 | |
| 4360 | MRC1 | mannose receptor C-type 1 | |
| 5621 | PRNP | prion protein (Kanno blood group) | |
| 60495 | HPSE2 | heparanase 2 (inactive) | |
| 90411 | MCFD2 | multiple coagulation factor deficiency 2, ER cargo receptor complex subunit |
Related Glycoprotein
