thrombophilia, X-linked, due to factor 8 defect
MONDO:0859082Mondo
Findings
No curated finding names thrombophilia, X-linked, due to factor 8 defect yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- X-linked inheritance
- Onset and course
- Middle age onset · Neonatal onset · Young adult onset
HPO, annotations 2026-09-02
Features
15 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Cerebral venous thrombosisHPOHP:0005305
- 1 of 1 reported patient
- Hepatic failureHPOHP:0001399
- 1 of 1 reported patient
- Increased factor VIII activityHPOHP:0030977
- 8 of 8 reported patients
- Left ventricular thrombusHPOHP:0040412
- 1 of 1 reported patient
- Portal hypertensionHPOHP:0001409
- 1 of 1 reported patient
- Portal vein thrombosisHPOHP:0030242
- 1 of 1 reported patient
- Recurrent deep vein thrombosisHPOHP:0004850
- 1 of 1 reported patient
- SeizureHPOHP:0001250
- 1 of 1 reported patient
- Splenic infarctionHPOHP:0034336
- 1 of 1 reported patient
- SplenomegalyHPOHP:0001744
- 1 of 1 reported patient
- StrokeHPOHP:0001297
- 1 of 1 reported patient
- Deep venous thrombosisHPOHP:0002625
- 4 of 6 reported patients
Show the remaining 3
- Pulmonary embolismHPOHP:0002204
- 3 of 6 reported patients
- Prolonged prothrombin timeHPOHP:0008151
- 2 of 7 reported patients
- Abnormality of von Willebrand factorHPOHP:0012146
- 0 of 7 reported patients
Where it sits
- A kind of