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 Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like PILAROWSKI-BJORNSSON SYNDROME; PILBOS MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2 BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES; BCYM4 CRYOHYDROCYTOSIS; CHC CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME; CACP PREMATURE AGING SYNDROME, PENTTINEN TYPE; PENTT SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48