Thrombophilia, Familial, Due To Decreased Release Of Tissue Plasminogen Activator; Thph9
Table of contents:
Genes related to Thrombophilia, Familial, Due To Decreased Release Of Tissue Plasminogen Activator; Thph9
- PLAT
Clinical Features
Phenotypes and symptoms related to Thrombophilia, Familial, Due To Decreased Release Of Tissue Plasminogen Activator; Thph9
- Pneumonia
- Venous thrombosis
- Thromboembolism
- Deep venous thrombosis
- Hypercoagulability
- Persistent bleeding after trauma
- Recurrent deep vein thrombosis
- Venous occlusion
- Hyperfibrinolysis
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Thrombophilia, Familial, Due To Decreased Release Of Tissue Plasminogen Activator; Thph9 Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 PLAT.
By Fulgent Genetics Fulgent Genetics (United States).
PLAT
Specificity
100 %
Genes
100 % |
You can get up to -7 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM MESH Rare Disease Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like STARGARDT DISEASE EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3; FHL3 AUTOSOMAL DOMINANT HYPERINSULINISM DUE TO KIR6.2 DEFICIENCY ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2 PEROXISOME BIOGENESIS DISORDER 14B; PEX14B