Kaposi Sarcoma
Description
Kaposi sarcoma (KS) is a rare human herpes virus 8 (HHV-8)-induced endothelial inflammatory neoplasm that develops is various clinically distinct settings, manifesting mostly as cutaneous lesions, or mucosal or visceral involvement.
Clinical Features
Top most frequent phenotypes and symptoms related to Kaposi Sarcoma
- Neoplasm
 - Hypertension
 - Fever
 - Fatigue
 - Edema
 - Diarrhea
 - Immunodeficiency
 - Encephalopathy
 - Pneumonia
 - Weight loss
 
And another 26 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Based on the latest data available KAPOSI SARCOMA have a estimated incidence of 0.34 per 100k worldwide.— No data available about the known clinical features onset.
Alternative names
Kaposi Sarcoma Is also known as multiple idiopathic pigmented hemangiosarcoma, susceptibility to.
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.Kaposi Sarcoma Recommended genes panels
| Panel Name, Specifity and genes Tested/covered | 
|---|
 	Crohn Disease.
By Bioscientia GmbH Center for Human Genetics (Germany). 
NOD2, IL6
 
Specificity
 
50 % 
Genes
 
100 %  | 
 	IL6.
By Fulgent Genetics Fulgent Genetics (United States). 
IL6
 
Specificity
 
100 % 
Genes
 
100 %  | 
 	OmniSeq Comprehensive.
By OmniSeq, Inc. (United States). 
RHEB, BCL9, ROS1, RPS6KB1, SF3B1, FOXL2, BRAF, BRCA1, BRCA2, SMARCB1, SMO, SOX2, SPOP, SRC, BTK, STAT3, STK11, HNF1A, TERT, TIAF1	, (...)
 
View the complete list with 122 more genes 
Specificity
 
1 % 
Genes
 
100 %  | 
 	Inflammatory Bowel Disease (IBD) and Related Disorders , Panel Massive Sequencing (NGS) 46 Genes.
By Reference Laboratory Genetics (Spain). 
SH2D1A, STXBP2, TERC, TERT, TGFB1, TINF2, CD40LG, WAS, WIPF1, CARD9, IL17F, IL23R, ADAM17, ATG16L1, CTLA4, WRAP53, CYBA, CYBB, DKC1, IRGM	, (...)
 
View the complete list with 24 more genes 
Specificity
 
3 % 
Genes
 
100 %  | 
You can get up to -4 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM ORPHANET Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL; CMS3A EPISODIC ATAXIA, TYPE 1; EA1 PEELING SKIN SYNDROME 2; PSS2 THROMBOPHILIA DUE TO THROMBOMODULIN DEFECT; THPH12 ATYPICAL WERNER SYNDROME DIAMOND-BLACKFAN ANEMIA 1; DBA1
	Crohn Disease.
	IL6.
	Inflammatory Bowel Disease (IBD) and Related Disorders , Panel Massive Sequencing (NGS) 46 Genes.