Kaposi Sarcoma

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

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.

Genes related to Kaposi Sarcoma

View recommended genes panels

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.

Click here to know more about Mendelian.

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 Panel complete gene list RHEB, BCL9, ROS1, RPS6KB1, SF3B1, FOXL2, BRAF, BRCA1, BRCA2, SMARCB1, SMO, SOX2, SPOP, SRC, BTK, STAT3, STK11, HNF1A, TERT, TIAF1, NKX2-1, MED12, TP53, TSC1, TSC2, U2AF1, VHL, WT1, XPO1, ZNF217, ATP11B, CBL, CCND1, CCNE1, NKX2-8, FBXW7, CD44, CDH1, ACVRL1, CD274, CDK4, CDK6, CDKN2A, DCUN1D1, PDCD1LG2, CSF1R, CSNK2A1, CTNNB1, TET2, DDR2, DNMT3A, KNSTRN, MYO18A, EGFR, ERBB2, ERBB3, ERBB4, ERG, ETV1, ETV4, ETV5, EZH2, FGFR1, FGFR2, FGFR3, FGFR4, FLT3, AKT1, AKT3, MTOR, GAS6, GATA2, GATA3, ALK, GNA11, GNAQ, GNAS, HRAS, IDH1, IDH2, IFITM1, IFITM3, IGF1R, APC, APEX1, BIRC2, BIRC3, IL6, JAK1, JAK2, JAK3, KDR, KIT, KRAS, AR, ARAF, RHOA, SMAD4, MAGOH, MAP2K1, MAP2K2, MAPK1, MAX, MCL1, MDM2, MDM4, MET, MLH1, MPL, MSH2, MYC, MYCL, MYCN, MYD88, ABL1, NF1, NF2, NFE2L2, NOTCH1, PNP, NPM1, ATM, NRAS, NTRK1, NTRK2, NTRK3, PAX5, PDGFRA, PIK3CA, PIK3R1, AXL, PPARG, PPP2R1A, BAP1, PTCH1, PTEN, PTPN11, RAC1, RAF1, RB1, BCL2L1, RET 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 Panel complete gene list SH2D1A, STXBP2, TERC, TERT, TGFB1, TINF2, CD40LG, WAS, WIPF1, CARD9, IL17F, IL23R, ADAM17, ATG16L1, CTLA4, WRAP53, CYBA, CYBB, DKC1, IRGM, FOXP1, ABCB1, GATA3, GUCY2C, NOD2, ICOS, XIAP, IKBKG, IL10, IL10RA, IL10RB, IL17RA, IL21, IL21R, IL2RA, IL2RG, IL6, FOXP3, MYO5B, NCF1, NCF2, NCF4, PLCG2, PTGER4 Specificity 3 % Genes 100 %

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Sources and references

You can check the following sources for additional information.

OMIM ORPHANET Rare Disease Symptoms Checker

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