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Bioinformatics and Systems Medicine Laboratory Bioinformatics and Systems Medicine Laboratory

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TissGeneSummary

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TissGeneExp

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TissGene-miRNA

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TissGeneMut: TissGeneSNV, TissGeneCNV, and TissGeneFusions

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TissGeneNet

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TissGeneProg

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TissGeneClin: TissGeneDrug and TissGeneDisease

TissGeneSummary for FGB
check button Gene summary
Basic gene informationGene symbolFGB
Gene namefibrinogen beta chain
SynonymsHEL-S-78p
CytomapUCSC genome browser: 4q28
Type of geneprotein-coding
RefGenesNM_001184741.1,
NM_005141.4,
Descriptionepididymis secretory sperm binding protein Li 78pfibrinogen, B beta polypeptide
Modification date20141222
dbXrefs MIM : 134830
HGNC : HGNC
HPRD : 00620
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_FGB
BioGPS: 2244
PathwayNCI Pathway Interaction Database: FGB
KEGG: FGB
REACTOME: FGB
Pathway Commons: FGB
ContextiHOP: FGB
ligand binding site mutation search in PubMed: FGB
UCL Cancer Institute: FGB
Assigned class in TissGDB*A
Included tissue-specific gene expression resourcesHPA,TiGER,GTEx
Specific-tissues in normal samples (assigned by TissGDB using HPA, TiGER, and GTEx)Liver
Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA)LIHC
Reference showing the relevant tissue of FGBCell type-specific differential induction of the human gamma-fibrinogen promoter by interleukin-6. Duan HO, Simpson-Haidaris PJ. J Biol Chem. 2006 May 5;281(18):12451-7. Epub 2006 Mar 8. (pmid:16524883)
go to article
Description by TissGene annotationsTissgsKTS
* Class A consists of genes with literature evidence and is part of the cTissGenes. Class B consists of only cTissGenes without additional evidence. The remaining genes belong to Class C.

check button Gene ontology having evidence of Inferred from Direct Assay (IDA) from Entrez
GO IDGO termPubMed ID
GO:0007160cell-matrix adhesion10903502
GO:0034116positive regulation of heterotypic cell-cell adhesion8100742
GO:0043623cellular protein complex assembly8910396
GO:0045907positive regulation of vasoconstriction15739255
GO:0045921positive regulation of exocytosis19193866
GO:0050714positive regulation of protein secretion19193866
GO:0051258protein polymerization12706644
GO:0051592response to calcium ion6777381
GO:0070374positive regulation of ERK1 and ERK2 cascade10903502
GO:0070527platelet aggregation6281794
GO:0090277positive regulation of peptide hormone secretion19193866
GO:1902042negative regulation of extrinsic apoptotic signaling pathway via death domain receptors10903502
GO:2000352negative regulation of endothelial cell apoptotic process10903502
GO:0007160cell-matrix adhesion10903502
GO:0034116positive regulation of heterotypic cell-cell adhesion8100742
GO:0043623cellular protein complex assembly8910396
GO:0045907positive regulation of vasoconstriction15739255
GO:0045921positive regulation of exocytosis19193866
GO:0050714positive regulation of protein secretion19193866
GO:0051258protein polymerization12706644
GO:0051592response to calcium ion6777381
GO:0070374positive regulation of ERK1 and ERK2 cascade10903502
GO:0070527platelet aggregation6281794
GO:0090277positive regulation of peptide hormone secretion19193866
GO:1902042negative regulation of extrinsic apoptotic signaling pathway via death domain receptors10903502
GO:2000352negative regulation of endothelial cell apoptotic process10903502


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TissGeneExp for FGB

check button Gene expressions across 28 cancer types (X-axis: cancer type and Y-axis: log2(norm_counts+1))
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
gene exp


check button Gene isoform expressions across 28 cancer types (X-axis: cancer type and Y-axis: log2(norm_counts+1))
(TCGA pan-cancer tcga_rsem_isoform_tpm, version 2016-09-01)
gene isoform exp


check button Gene expressions across normal tissues of GTEx data
(GTEx GTEx_Analysis_v6_RNA-seq_RNA-SeQCv1.1.8_gene_rpkm.gct)
- Here, we shows the matched tissue types only among our 28 cancer types.
normal gene exp


check button Different expressions across 14 cancer types with more than 10 samples between matched tumors and normals (X-axis: cancer type and Y-axis: log2(norm_counts+1))
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
DEG exp

- Significantly differentially expressed cancer types and information. (|Fold change|>1 and FDR<0.05)
Cancer typeMean(exp) in tumorMean(exp) in matched normalLog2FCP-val.FDR
KICH-1.7854702353.490353765-5.2758241.97E-089.96E-08
LUAD2.473933075-0.3533772692.8273103452.47E-056.85E-05
LIHC14.2995657716.82209977-2.5225346.53E-096.02E-08
KIRP1.603025643.78946939-2.186443750.01950.039636446
COAD-0.344473158-1.9177693121.5732961540.0005220.001599583


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TissGene-miRNA for FGB

check button Significantly anti-correlated miRNAs of TissGene across 28 cancer types
(Gene-miRNA relations from TargetScanHuman Relsease 7.1, Conserved_Site_Context_Scores.txt.zip, 06.01.2016)
(TCGA IlluminaHiSeq_miRNASeq, log2(RPM+1) data, version 2016-11-21)
(TCGA IlluminaHiSeq_RNASeqV2, log2(normalized_count+1) data, version 2016-08-16)
(Spearman’s Rank Correlation (p-value<0.05 and coefficient<-0.25))
Cancer typemiRNA idmiRNA accessionP-val.Coeff.# samples


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TissGeneMut for FGB
TissGeneSNV for FGB

check button nsSNV counts per each loci.
Different colors of circles represent different cancer types. Circle size denotes number of samples.
(TCGA somatic mutation (SNPs and small INDELs) data, version 2016-04-25)

* Click on the image to enlarge it in a new window.
SNV lollipop
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check button Somatic nucleotide variants of TissGene across 28 cancer types
(X-axis: cancer type and Y-axis: % of mutated samples)
The numbers in parentheses are numbers of samples with mutation (nsSNVs).
(TCGA somatic mutation (SNPs and small INDELs) data, version 2016-04-25)
SNV distribution

- nsSNVs sorted by frequency.
AAchangeCancer type# samples
p.R47QSKCM2
p.E339QLUAD2
p.K328TUCS1
p.G444SCOAD1
p.K211RUCEC1
p.R199CSKCM1
p.R267*HNSC1
p.R87IBLCA1
p.R72WBLCA1
p.D419YOV1
p.Y182HESCA1
p.D327NBRCA1
p.P90TPAAD1
p.G472EOV1
p.K471NUCEC1
p.V361LLUAD1
p.P122QBLCA1
p.M468ISKCM1
p.R74HSTAD1
p.D455ETHYM1
p.L340RSTAD1
p.A136DPAAD1
p.E243KLUAD1
p.W279LOV1
p.N125SSARC1
p.D463NSKCM1
p.A89DLUAD1
p.Q82EBLCA1
p.D350NLIHC1
p.S371LHNSC1
p.D164_spliceGBM1
p.R199CREAD1
p.R74HKICH1
p.A79VKICH1
p.M482RBLCA1
p.G39DSKCM1
p.E253DUCEC1
p.R124GSTAD1
p.G248RSARC1
p.R224CUCEC1
p.D411YPRAD1
p.S126TSKCM1
p.R87KSKCM1
p.Q331LLUAD1
p.D164YLUAD1
p.S142CLUAD1
p.A382VGBM1
p.L341SLUSC1
p.H355QPAAD1
p.T407MGBM1
p.V361LUCEC1
p.N125SLIHC1
p.K328NSTAD1
p.P100SSKCM1
p.W323LLUAD1
p.S237PUCEC1
p.G317CLUAD1
p.R196CREAD1
p.W454LCHOL1
p.E275KLUSC1
p.G402SSTAD1
p.R44CMESO1
p.K471RSKCM1
p.G349ELUAD1
p.T407MLGG1
p.L324IPRAD1
p.S473TLUAD1
p.A98TUCS1
p.M397VHNSC1
p.D327NSKCM1
p.N469HESCA1
p.K178NLUSC1
p.G450ELUAD1
p.Q146*HNSC1
p.E129DLUSC1
p.K313NPAAD1
p.C95SLUAD1
p.H438NUCEC1
p.W448CTHYM1
p.E250*LUAD1
p.E343*UCEC1


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TissGeneCNV for FGB

check button Copy number variations of TissGene across 28 cancer types (X-axis: cancer type and Y-axis: % of CNV samples)
(TCGA Gistic2_CopyNumber_Gistic2_all_data_by_genes, Gistic2 copy number data, version 2016-08-16)
CNV


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TissGeneFusions for FGB

check button Fusion genes including TissGene
(ChimerDB 3.0, 2016-12-01 and TCGA fusion Portal 2015-12-01)
DatabaseSrcCancer typeSampleFusion geneORF5'-gene BP3'-gene BP
Chimerdb3.0ChiTaRsNAAI065122FGB-FGBchr4:155491723chr4:155488755
Chimerdb3.0ChiTaRsNABC020762FGB-GNASchr4:155490429chr20:57485039
Chimerdb3.0ChiTaRsNAAW970840FGB-FGBchr4:155492174chr4:155492186
Chimerdb3.0ChiTaRsNAAA491846FGB-FGBchr4:155492174chr4:155492184
Chimerdb3.0ChiTaRsNABG568132ZFP36L1-FGBchr14:69255154chr4:155491882
TCGAfusionPortalPRADABRCATCGA-D8-A13Z-01AARFIP1-FGBIn-frameChr4:153750878Chr4:155486960
TCGAfusionPortalPRADALUADTCGA-78-7148-01AFGB-PLEKHA5NAChr4:155492238Chr12:19441012


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TissGeneNet for FGB

check button Co-expressed gene networks based on protein-protein interaction data (CePIN)
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(PINA2 ppi data)
BRCA (tumor)BRCA (normal)
FGB, CDKN1A, SMN1, TK1, NID1, ANXA7, GRB7, PITX3, CALR, HNF1A, KHDRBS2, F2, SERPINA5, FGA, RORA, AIMP2, FBLN1, FGG, PIK3R3, FOXA2, KLK6 (tumor)FGB, CDKN1A, SMN1, TK1, NID1, CEBPB, ANXA7, GRB7, CSNK2B, CALR, HNF1A, KHDRBS2, LPA, F2, FGA, AIMP2, FBLN1, FGG, PIK3R3, MIS12, KLK6 (normal)
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COAD (tumor)COAD (normal)
FGB, CDKN1A, SMN1, TK1, NID1, ANXA7, GRB7, PITX3, CSNK2B, CALR, KHDRBS2, LPA, F2, SERPINA5, FGA, RORA, FBLN1, FGG, PIK3R3, MIS12, KLK6 (tumor)FGB, CDKN1A, SMN1, TK1, CEBPB, ANXA7, PITX3, CALR, HNF1A, KHDRBS2, LPA, F2, SERPINA5, FGA, RORA, AIMP2, FBLN1, FGG, PIK3R3, FOXA2, KLK6 (normal)
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HNSC (tumor)HNSC (normal)
FGB, CDKN1A, SMN1, TK1, NID1, CEBPB, ANXA7, PITX3, CSNK2B, CALR, HNF1A, KHDRBS2, F2, SERPINA5, FGA, AIMP2, FBLN1, FGG, MIS12, FOXA2, KLK6 (tumor)FGB, CDKN1A, SMN1, NID1, CEBPB, ANXA7, PITX3, CSNK2B, HNF1A, LPA, F2, SERPINA5, FGA, RORA, AIMP2, FBLN1, FGG, PIK3R3, MIS12, FOXA2, KLK6 (normal)
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KICH (tumor)KICH (normal)
FGB, CDKN1A, TK1, NID1, CEBPB, ANXA7, GRB7, PITX3, CSNK2B, CALR, HNF1A, KHDRBS2, LPA, F2, FGA, FBLN1, FGG, PIK3R3, MIS12, FOXA2, KLK6 (tumor)FGB, CDKN1A, SMN1, TK1, NID1, ANXA7, GRB7, CSNK2B, CALR, HNF1A, KHDRBS2, SERPINA5, FGA, RORA, AIMP2, FBLN1, FGG, PIK3R3, MIS12, FOXA2, KLK6 (normal)
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KIRC (tumor)KIRC (normal)
FGB, SMN1, TK1, NID1, CEBPB, ANXA7, GRB7, PITX3, CSNK2B, CALR, HNF1A, KHDRBS2, LPA, F2, SERPINA5, FGA, FGG, PIK3R3, MIS12, FOXA2, KLK6 (tumor)FGB, CDKN1A, TK1, NID1, CEBPB, GRB7, PITX3, CSNK2B, CALR, HNF1A, KHDRBS2, LPA, F2, SERPINA5, FGA, AIMP2, FBLN1, FGG, PIK3R3, FOXA2, KLK6 (normal)
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KIRP (tumor)KIRP (normal)
FGB, TK1, NID1, CEBPB, ANXA7, GRB7, PITX3, CALR, HNF1A, KHDRBS2, LPA, F2, SERPINA5, FGA, RORA, AIMP2, FBLN1, FGG, PIK3R3, FOXA2, KLK6 (tumor)FGB, CDKN1A, NID1, CEBPB, GRB7, PITX3, CSNK2B, CALR, KHDRBS2, LPA, F2, SERPINA5, FGA, RORA, AIMP2, FBLN1, FGG, PIK3R3, MIS12, FOXA2, KLK6 (normal)
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LIHC (tumor)LIHC (normal)
FGB, CDKN1A, TK1, NID1, CEBPB, GRB7, PITX3, CALR, HNF1A, KHDRBS2, LPA, F2, SERPINA5, FGA, RORA, AIMP2, FBLN1, FGG, PIK3R3, MIS12, FOXA2 (tumor)FGB, CDKN1A, SMN1, TK1, NID1, CEBPB, ANXA7, PITX3, CALR, HNF1A, KHDRBS2, LPA, F2, SERPINA5, FGA, RORA, FBLN1, FGG, PIK3R3, FOXA2, KLK6 (normal)
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LUAD (tumor)LUAD (normal)
FGB, CDKN1A, SMN1, TK1, NID1, CEBPB, ANXA7, GRB7, PITX3, CSNK2B, CALR, HNF1A, F2, SERPINA5, FGA, RORA, AIMP2, FGG, PIK3R3, MIS12, FOXA2 (tumor)FGB, CDKN1A, TK1, NID1, CEBPB, ANXA7, GRB7, PITX3, CSNK2B, CALR, HNF1A, F2, FGA, RORA, AIMP2, FBLN1, FGG, PIK3R3, MIS12, FOXA2, KLK6 (normal)
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LUSC (tumor)LUSC (normal)
FGB, CDKN1A, SMN1, TK1, NID1, CEBPB, GRB7, PITX3, CSNK2B, CALR, HNF1A, KHDRBS2, F2, FGA, RORA, AIMP2, FBLN1, FGG, PIK3R3, FOXA2, KLK6 (tumor)FGB, CDKN1A, TK1, CEBPB, ANXA7, PITX3, CSNK2B, CALR, HNF1A, KHDRBS2, LPA, F2, SERPINA5, FGA, RORA, AIMP2, FBLN1, FGG, PIK3R3, FOXA2, KLK6 (normal)
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PRAD (tumor)PRAD (normal)
FGB, CDKN1A, SMN1, NID1, CEBPB, GRB7, PITX3, CSNK2B, CALR, HNF1A, KHDRBS2, F2, SERPINA5, FGA, RORA, AIMP2, FBLN1, FGG, PIK3R3, FOXA2, KLK6 (tumor)FGB, CDKN1A, TK1, CEBPB, ANXA7, GRB7, PITX3, CSNK2B, CALR, HNF1A, KHDRBS2, LPA, F2, SERPINA5, FGA, RORA, AIMP2, FGG, MIS12, FOXA2, KLK6 (normal)
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STAD (tumor)STAD (normal)
FGB, CDKN1A, TK1, NID1, ANXA7, GRB7, CSNK2B, CALR, HNF1A, LPA, F2, SERPINA5, FGA, RORA, AIMP2, FBLN1, FGG, PIK3R3, MIS12, FOXA2, KLK6 (tumor)FGB, NID1, CEBPB, ANXA7, GRB7, PITX3, CSNK2B, CALR, HNF1A, KHDRBS2, LPA, F2, SERPINA5, FGA, RORA, AIMP2, FGG, PIK3R3, MIS12, FOXA2, KLK6 (normal)
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THCA (tumor)THCA (normal)
FGB, CDKN1A, TK1, NID1, CEBPB, ANXA7, GRB7, PITX3, CALR, HNF1A, KHDRBS2, LPA, F2, SERPINA5, FGA, RORA, FBLN1, FGG, MIS12, FOXA2, KLK6 (tumor)FGB, SMN1, TK1, NID1, CEBPB, ANXA7, GRB7, PITX3, CSNK2B, HNF1A, KHDRBS2, LPA, F2, SERPINA5, FGA, RORA, AIMP2, FGG, PIK3R3, MIS12, KLK6 (normal)
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TissGeneProg for FGB

check button Kaplan-Meier plots with logrank tests of overall survival (OS) using 28 cancer types
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(TCGA clinicalMatrix, phenotype data, version 2016-04-27)

* Click on the image to enlarge it in a new window.
survival 1

check button Kaplan-Meier plots with logrank test of relapse free survival (RFS) using 28 cancer types
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(TCGA clinicalMatrix, phenotype data, version 2016-04-27)

* Click on the image enlarge it in a new window.
survival 2

check button Forest plot of Cox proportional hazard ratio (HR) and 95% CI of overall survival (OS) using 28 cancer types
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(TCGA clinicalMatrix, phenotype data, version 2016-04-27)

* Click on the image enlarge it in a new window.
survival 3

check button Forest plot of Cox proportional hazard ratio (HR) and 95% CI of relapse free survival (RFS) using 28 cancer types
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(TCGA clinicalMatrix, phenotype data, version 2016-04-27)

* Click on the image enlarge it in a new window.
survival 4

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TissGeneClin for FGB
TissGeneDrug for FGB

check button Drug information targeting TissGene
(DrugBank Version 5.0.6, 2017-04-01)
DrugBank IDDrug nameDrug activityDrug typeDrug status


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TissGeneDisease for FGB

check button Disease information associated with TissGene
(DisGeNet, 2016-06-01)
Disease IDDisease name# pubmedsSource
umls:C0027051Myocardial Infarction22BeFree,GAD,LHGDN
umls:C1561955Fibrinogen Adverse Event21GAD,GWASCAT
umls:C0038454Cerebrovascular accident16BeFree,GAD,LHGDN
umls:C0948008Ischemic stroke12BeFree,GAD
umls:C0007222Cardiovascular Diseases11BeFree,GAD,LHGDN
umls:C0020538Hypertensive disease10BeFree,GAD,LHGDN
umls:C0040053Thrombosis8GAD,LHGDN
umls:C0007786Brain Ischemia7GAD
umls:C0004153Atherosclerosis6BeFree,GAD
umls:C0001733Afibrinogenemia5BeFree,CTD_human,LHGDN
umls:C0007785Cerebral Infarction5GAD,LHGDN
umls:C0010068Coronary heart disease4BeFree,GAD
umls:C0019250Hereditary factor I deficiency disease4BeFree
umls:C0042373Vascular Diseases4GAD,LHGDN
umls:C0042487Venous Thrombosis4GAD
umls:C0149871Deep Vein Thrombosis4BeFree,GAD
umls:C0151744Myocardial Ischemia4GAD
umls:C1956346Coronary Artery Disease4BeFree,GAD,LHGDN
umls:C2584774Congenital hypofibrinogenemia4ORPHANET,UNIPROT
umls:C3272363Ischemic Cerebrovascular Accident4BeFree
umls:C0004238Atrial Fibrillation3GAD
umls:C0007789Cerebral Palsy3GAD
umls:C0010054Coronary Arteriosclerosis3BeFree,GAD
umls:C0028754Obesity3GAD
umls:C0034065Pulmonary Embolism3GAD,RGD
umls:C0398623Thrombophilia3GAD
umls:C0948089Acute Coronary Syndrome3GAD
umls:C1861172Venous Thromboembolism3GAD
umls:C0001925Albuminuria2GAD
umls:C0002895Anemia, Sickle Cell2GAD
umls:C0007273Carotid Artery Diseases2BeFree,GAD
umls:C0010072Coronary Thrombosis2GAD
umls:C0011860Diabetes Mellitus, Non-Insulin-Dependent2GAD
umls:C0021368Inflammation2GAD
umls:C0022661Kidney Failure, Chronic2BeFree,GAD
umls:C0024143Lupus Nephritis2BeFree,GAD,LHGDN
umls:C0031099Periodontitis2GAD
umls:C0035326Retinal vascular occlusion2GAD
umls:C0085096Peripheral Vascular Diseases2GAD
umls:C0243026Sepsis2GAD,LHGDN
umls:C0266929Chronic Periodontitis2GAD
umls:C0553681Hypofibrinogenemia2BeFree
umls:C0687675Pregnancy loss2GAD
umls:C0852077Blood Coagulation Disorders, Inherited2GAD
umls:C0000809Abortion, Habitual1GAD
umls:C0002382Alveolar Bone Loss1GAD
umls:C0002395Alzheimer's Disease1GAD
umls:C0002736Amyotrophic Lateral Sclerosis1GAD
umls:C0002962Angina Pectoris1GAD
umls:C0002965Angina, Unstable1BeFree
umls:C0003850Arteriosclerosis1BeFree
umls:C0003873Rheumatoid Arthritis1GAD
umls:C0005283beta Thalassemia1GAD
umls:C0007282Carotid Stenosis1GAD
umls:C0007820Cerebrovascular Disorders1GAD
umls:C0008495Chorioamnionitis1GAD
umls:C0015944Fetal Membranes, Premature Rupture1GAD
umls:C0017327Generalized atherosclerosis1GAD
umls:C0019080Hemorrhage1GAD
umls:C0020542Pulmonary Hypertension1GAD
umls:C0021361Female infertility1GAD
umls:C0021390Inflammatory Bowel Diseases1GAD
umls:C0022116Ischemia1GAD
umls:C0022658Kidney Diseases1GAD
umls:C0022876Premature Obstetric Labor1GAD
umls:C0023234Legg-Calve-Perthes Disease1GAD,LHGDN
umls:C0024117Chronic Obstructive Airway Disease1GAD
umls:C0024131Lupus Vulgaris1GAD
umls:C0024138Lupus Erythematosus, Discoid1GAD
umls:C0024141Lupus Erythematosus, Systemic1GAD
umls:C0026269Mitral Valve Stenosis1GAD
umls:C0026691Mucocutaneous Lymph Node Syndrome1GAD
umls:C0026837Muscle Rigidity1BeFree
umls:C0029456Osteoporosis1CTD_human
umls:C0030305Pancreatitis1RGD
umls:C0030567Parkinson Disease1CTD_human
umls:C0031094Periodontal Pocket1GAD
umls:C0031106Periodontitis, Juvenile1GAD
umls:C0032914Pre-Eclampsia1GAD
umls:C0035078Kidney Failure1BeFree
umls:C0036421Systemic Scleroderma1GAD
umls:C0040038Thromboembolism1GAD
umls:C0151526Premature Birth1GAD
umls:C0151942Arterial thrombosis1BeFree
umls:C0155626Acute myocardial infarction1BeFree
umls:C0155668Old myocardial infarction1BeFree
umls:C0206114Periodontal Attachment Loss1GAD
umls:C0242383Age related macular degeneration1GAD
umls:C0272350Dysfibrinogenemia, Congenital1ORPHANET,UNIPROT
umls:C0333186Restenosis1GAD
umls:C0340293Anterior myocardial infarction1BeFree
umls:C0342257Complications of Diabetes Mellitus1GAD
umls:C0409974Lupus Erythematosus1GAD
umls:C0524620Metabolic Syndrome X1GAD
umls:C0856169Endothelial dysfunction1BeFree
umls:C0856761Budd-Chiari Syndrome1GAD
umls:C1261287Stenosis1LHGDN
umls:C1272641Systemic arterial pressure1GAD
umls:C1842372ASPIRIN RESISTANCE1GAD
umls:C2919032Infection of amniotic sac and membranes, unspecified, unspecified trimester, not applicable or unspecified1GAD
umls:C2921106Recurrent pregnancy loss1GAD
umls:C3178801Stroke, Lacunar1GAD