Inflammatory Bowel Disease (crohn Disease) 1; Ibd1

Table of contents:

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

Genes related to Inflammatory Bowel Disease (crohn Disease) 1; Ibd1

IL6
NOD2

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Inflammatory Bowel Disease (crohn Disease) 1; Ibd1

Growth delay
Neoplasm
Diarrhea
Abdominal pain
Weight loss
Psoriasiform dermatitis
Intestinal obstruction
Inflammation of the large intestine
Colon cancer
Colitis

And another 8 symptoms. If you need more information about this disease we can help you.

Click here to know more about Mendelian.

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.

Inflammatory Bowel Disease (crohn Disease) 1; Ibd1 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Crohn Disease. By Bioscientia GmbH Center for Human Genetics (Germany). NOD2, IL6 Specificity 100 % Genes 100 %
IL6. By Fulgent Genetics Fulgent Genetics (United States). IL6 Specificity 100 % Genes 50 %
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 50 %
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 5 % Genes 100 %
Blau Syndrome (NOD2/CARD15 Complete Gene). By Center for Genetics at Saint Francis Saint Francis Hospital (United States). NOD2 Specificity 100 % Genes 50 %
Crohn's Disease - NOD2/CARD15 Complete Gene Analysis. By Center for Genetics at Saint Francis Saint Francis Hospital (United States). NOD2 Specificity 100 % Genes 50 %
NOD2 Deletion/duplication analysis. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). NOD2 Specificity 100 % Genes 50 %
NOD2 Sequencing. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). NOD2 Specificity 100 % Genes 50 %

You can get up to 41 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM ORPHANET Genetic Syndrome Finder

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11 HARTNUP DISORDER; HND MYOPATHY, DISTAL, 4; MPD4 ANDROGEN INSENSITIVITY SYNDROME; AIS LYMPHEDEMA, HEREDITARY, IC; LMPH1C