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 TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, AND OTHER ABNORMALITIES OROFACIODIGITAL SYNDROME XIV; OFD14 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2 ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS2 SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48 MICROPHTHALMIA, SYNDROMIC 12; MCOPS12