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hemophilia B
Summary
- Synonym
-
- Congenital factor IX deficiency
- Congenital factor IX disorder
- deficiency, functional factor IX
- factor IX deficiency
- Definition
- A blood coagulation disease that has_material_basis_in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait.
- Super Class
- X-linked recessive disease blood coagulation disease
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 275 | AMT | aminomethyltransferase | |
| 952 | CD38 | CD38 molecule | |
| 2539 | G6PD | glucose-6-phosphate dehydrogenase | |
| 2571 | GAD1 | glutamate decarboxylase 1 | |
| 10682 | EBP | EBP cholestenol delta-isomerase | |
| 22908 | SACM1L | SAC1 like phosphatidylinositide phosphatase | |
| 23583 | SMUG1 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | |
| 51181 | DCXR | dicarbonyl and L-xylulose reductase |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P11413 | Glucose-6-phosphate 1-dehydrogenase | |
| P28907 | ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 | |
| Q15125 | 3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase | |
| Q7Z4W1 | L-xylulose reductase |
