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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 ITGB3
check button Gene summary
Basic gene informationGene symbolITGB3
Gene nameintegrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
SynonymsBDPLT16|BDPLT2|CD61|GP3A|GPIIIa|GT
CytomapUCSC genome browser: 17q21.32
Type of geneprotein-coding
RefGenesNM_000212.2,
Descriptionintegrin beta-3platelet membrane glycoprotein IIIa
Modification date20141222
dbXrefs MIM : 173470
HGNC : HGNC
Ensembl : ENSG00000259207
HPRD : 01428
Vega : OTTHUMG00000171956
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_ITGB3
BioGPS: 3690
PathwayNCI Pathway Interaction Database: ITGB3
KEGG: ITGB3
REACTOME: ITGB3
Pathway Commons: ITGB3
ContextiHOP: ITGB3
ligand binding site mutation search in PubMed: ITGB3
UCL Cancer Institute: ITGB3
Assigned class in TissGDB*C
Included tissue-specific gene expression resourcesTiGER,GTEx
Specific-tissues in normal samples (assigned by TissGDB using HPA, TiGER, and GTEx)KidneyThyroid gland
Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA)KIRC,KIRP,KICHTHCA
Reference showing the relevant tissue of ITGB3
Description by TissGene annotationsCancer gene
Fused withTSGene
* 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:0006457protein folding12204115
GO:0007160cell-matrix adhesion22505472
GO:0007229integrin-mediated signaling pathway23382103
GO:0034446substrate adhesion-dependent cell spreading24658351
GO:0006457protein folding12204115
GO:0007160cell-matrix adhesion22505472
GO:0007229integrin-mediated signaling pathway23382103
GO:0034446substrate adhesion-dependent cell spreading24658351


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TissGeneExp for ITGB3

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
PRAD-0.1841321820.976440895-1.1605730775.72E-074.32E-06
BLCA-0.9405939230.942774498-1.8833684210.003750.02127551
COAD-0.1343052591.23627551-1.3705807690.0002330.000780586
KICH1.0277839722.505783972-1.4784.05E-050.000114292


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TissGene-miRNA for ITGB3

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 ITGB3
TissGeneSNV for ITGB3

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.S395FSKCM2
p.R441CSKCM2
p.W406*SKCM1
p.C64SLUAD1
p.D205ASTAD1
p.E697KSKCM1
p.E501KBLCA1
p.R750QREAD1
p.V691ISTAD1
p.R750QSKCM1
p.S393PLIHC1
p.M144ILUAD1
p.S411YUCEC1
p.P377TSKCM1
p.R505HLUSC1
p.S638GLGG1
p.G273RSKCM1
p.I170VLIHC1
p.R505CSKCM1
p.P105SSKCM1
p.N597DBRCA1
p.R505LESCA1
p.R378CUCEC1
p.R169*LGG1
p.E200KSKCM1
p.E548KCESC1
p.D54NLUAD1
p.L600QLUAD1
p.L744PLIHC1
p.F396LCESC1
p.L350PLGG1
p.L343FSKCM1
p.G637RKIRC1
p.R524WDLBC1
p.S47FSKCM1
p.D653NSKCM1
p.S507FSKCM1
p.E338KTHCA1
p.S536NSTAD1
p.P111HCOAD1
p.S194FSKCM1
p.R487CLUSC1
p.P628QLUAD1
p.G418EHNSC1
p.K558NLIHC1
p.E81KBLCA1
p.R176WUCEC1
p.W406*HNSC1
p.P155SLUAD1
p.R514*STAD1
p.S348NUCEC1
p.R63HPAAD1
p.W477*SKCM1
p.A289TUCEC1
p.S61LHNSC1
p.S563*LUAD1
p.A164ELUAD1
p.G605STGCT1
p.K410EUCEC1
p.R750*SKCM1
p.S326FSKCM1
p.D647GLGG1
p.R63HTHYM1
p.Q454PUCEC1
p.D122YLUSC1
p.R386CSTAD1
p.W492*UCEC1
p.D135NSKCM1
p.H300YESCA1
p.S123LBRCA1
p.P366SSKCM1
p.D152NSKCM1
p.L731VBLCA1
p.R386CBLCA1
p.A754TSARC1
p.H138YSKCM1
p.K124QSKCM1
p.S439FKIRP1
p.N365SBRCA1
p.A283PHNSC1
p.R750XSKCM1
p.R750QUCEC1
p.D749HCESC1
p.R742CLUAD1
p.S127CLUAD1
p.A478TSKCM1
p.W554*SKCM1
p.I744VSKCM1
p.Y344*LIHC1
p.P628HLUAD1
p.R34LMESO1
p.H349YSKCM1
p.R515WSTAD1
p.G418ESKCM1
p.R589CGBM1
p.E752*UCEC1
p.Y773HBLCA1
p.E608KSKCM1
p.A255DLUAD1
p.T590SLUAD1
p.P389SSKCM1
p.D184EKIRP1
p.T784MBLCA1
p.G172RSKCM1
p.R589CBLCA1
p.R740GSTAD1
p.E664KUCEC1
p.Q108RSKCM1
p.D362YHNSC1
p.G566SSKCM1
p.R648QBLCA1
p.S79FSKCM1
p.D510NSKCM1
p.E654KSKCM1
p.I252TLIHC1
p.H617NLUAD1
p.Y578*LUAD1
p.E68DREAD1
p.R422SHNSC1
p.S363TLUSC1
p.G435DSKCM1
p.R786QCOAD1
p.H145YHNSC1
p.E511KSKCM1
p.D749NSKCM1
p.T420MHNSC1


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TissGeneCNV for ITGB3

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 ITGB3

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
Chimerdb3.0ChiTaRsNABI059143GOLGA1-ITGB3chr9:127642395chr17:45335169
Chimerdb3.0ChiTaRsNAAI655822KIF4A-ITGB3chrX:69542274chr17:45390262
Chimerdb3.0ChiTaRsNAAU116912ITGB3-INADLchr17:45389761chr1:62617829
Chimerdb3.0ChiTaRsNABC015906ITGB3-FMN1chr17:45390031chr15:33062085
Chimerdb3.0ChiTaRsNABF800064ITGB3-TTC12chr17:45421652chr11:113230098
Chimerdb3.0ChiTaRsNAT11184SCG3-ITGB3chr15:51973975chr17:45381930
Chimerdb3.0FusionScanESCATCGA-L5-A4OH-01ASPOP-ITGB35'UTR-CDSchr17:47755294chr17:45351784
Chimerdb3.0FusionScanOVTCGA-24-1103-01AITGB3-DYNLRB1In-Framechr17:45331306chr20:33122431


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TissGeneNet for ITGB3

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)
ITGB3, NID1, FN1, PTPN11, KDR, ITGAV, NFATC2, EPS8, PECAM1, DAB2, PDGFRB, COL1A2, PBX2, TGM2, CD36, TLN1, TENC1, FBLN2, PDGFRA, ITGA5, THY1 (tumor)ITGB3, NID1, FN1, FLNA, PTPN11, KDR, ITGAV, NFATC2, THBS1, EPS8, DAB2, PDGFRB, COL1A2, TLN1, NUMB, PDPK1, FBLN2, PDGFRA, GULP1, ITGA5, THY1 (normal)
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COAD (tumor)COAD (normal)
ITGB3, NID1, FN1, FLNA, PTPN11, AKT1, ILK, PDGFRB, COL1A2, MAPK8IP1, RABGAP1, PBX2, CIB1, TLN1, NUMB, ANKS1B, TENC1, PTPRZ1, ITGA5, P2RY2, THY1 (tumor)ITGB3, NID1, FN1, FLNA, KDR, ITGAV, NFATC2, THBS1, PECAM1, PDGFRB, COL1A2, TGM2, CD36, TLN1, TENC1, NFATC1, FBLN2, PDGFRA, PTPRZ1, ITGA5, THY1 (normal)
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HNSC (tumor)HNSC (normal)
ITGB3, NID1, SYK, FN1, KDR, ITGAV, THBS1, PECAM1, DAB2, PDGFRB, COL1A2, CDCA8, CD36, TLN1, CAPN1, ANKS1B, TENC1, NFATC1, FBLN2, PDGFRA, ITGA5 (tumor)ITGB3, NID1, FN1, FLNA, PTPN11, KDR, ITGAV, NFATC2, THBS1, EPS8, DAB2, PDGFRB, COL1A2, TGM2, TLN1, TENC1, FBLN2, PDGFRA, ITGA5, THY1, MYO10 (normal)
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KICH (tumor)KICH (normal)
ITGB3, SRC, SHC1, FLNA, PTPN1, PTPN11, YES1, ITGAV, THBS1, DAB2, PTK2B, PDGFRB, COL1A2, FGA, VTN, CD36, TLN1, FGG, RGS12, ITGA2B, P2RY2 (tumor)ITGB3, FLNB, NID1, FN1, FLNA, PTPN11, ITGAV, PTK2, THBS1, EPS8, DAB2, PTK2B, TGM2, CD36, PDPK1, FGG, NFATC1, ITGA2B, FBLN2, GULP1, ITGA5 (normal)
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KIRC (tumor)KIRC (normal)
ITGB3, NID1, SYK, SHC1, FLNA, PTPN1, PTPN11, KDR, ITGAV, THBS1, EPS8, DAB2, PDGFRB, COL1A2, PXN, FGA, TLN1, CEACAM1, ITGA2B, GULP1, ITGA5 (tumor)ITGB3, NID1, FN1, FLNA, PTPN1, PTPN11, LYN, YES1, ITGAV, NFATC2, PTK2, THBS1, EPS8, COL1A2, MAPK8IP1, TGM2, TLN1, PDPK1, FBLN2, ITGA5, MYO10 (normal)
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KIRP (tumor)KIRP (normal)
ITGB3, NID1, SYK, SHC1, PTPN1, PTPN11, KDR, ITGAV, THBS1, EPS8, DAB2, PDGFRB, PXN, MAPK8IP1, FGA, MAP3K13, TLN1, FGG, ITGA2B, FBLN2, GULP1 (tumor)ITGB3, NID1, SHC1, FN1, FLNA, PTPN1, ITGAV, NFATC2, PTK2, THBS1, EPS8, RABGAP1, TGM2, CIB1, FGA, MAP3K13, TLN1, ANKS1B, PDPK1, FGG, GULP1 (normal)
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LIHC (tumor)LIHC (normal)
ITGB3, NID1, SYK, PTPN1, PTPN11, KDR, YES1, ITGAV, NFATC2, PTK2, EPS8, DAB2, RABGAP1, CIB1, VTN, CD36, MAP3K13, TLN1, NUMB, PDGFRA, MYO10 (tumor)ITGB3, NID1, FN1, FLNA, PTPN1, PTPN11, KDR, YES1, ITGAV, NFATC2, AKT1, EPS8, PTK2B, COL1A2, CIB1, DAB1, MAP3K13, TLN1, NUMB, PDPK1, FBLN2 (normal)
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LUAD (tumor)LUAD (normal)
ITGB3, FLNB, NID1, FN1, FLNA, PTPN11, KDR, ITGAV, NFATC2, THBS1, PDGFRB, PXN, TLN1, ANKS1B, DOK1, NFATC1, ITGA2B, FBLN2, PDGFRA, PTPRZ1, ITGA5 (tumor)ITGB3, NID1, FN1, FLNA, LYN, KDR, ITGAV, NFATC2, THBS1, DAB2, PDGFRB, COL1A2, TGM2, FGA, MAP3K13, TLN1, NFATC1, FBLN2, PDGFRA, ITGA5, THY1 (normal)
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LUSC (tumor)LUSC (normal)
ITGB3, NID1, SHC1, FN1, FLNA, PTPN11, KDR, ITGAV, NFATC2, THBS1, DAB2, PDGFRB, COL1A2, TGM2, CIB1, TLN1, NFATC1, ITGA2B, FBLN2, ITGA5, MYO10 (tumor)ITGB3, NID1, FN1, FLNA, KDR, ITGAV, NFATC2, THBS1, ILK, PECAM1, DAB2, PDGFRB, COL1A2, PXN, TGM2, TLN1, TENC1, FBLN2, PDGFRA, ITGA5, THY1 (normal)
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PRAD (tumor)PRAD (normal)
ITGB3, NID1, FN1, FLNA, PTPN11, KDR, NFATC2, ILK, DAB2, PDGFRB, COL1A2, RABGAP1, CIB1, DAB1, CD36, TLN1, ANKS1B, TENC1, PDGFRA, ITGA5, THY1 (tumor)ITGB3, NID1, FN1, FLNA, PTPN11, KDR, NFATC2, THBS1, EPS8, DAB2, PDGFRB, COL1A2, RABGAP1, CIB1, DAB1, TLN1, NUMB, FBLN2, PDGFRA, ITGA5, P2RY2 (normal)
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STAD (tumor)STAD (normal)
ITGB3, NID1, FN1, FLNA, PTPN11, ITGAV, PTK2, AKT1, ILK, PDGFRB, COL1A2, CDCA8, MAPK8IP1, TGM2, TLN1, TENC1, NFATC1, FBLN2, PDGFRA, ITGA5, THY1 (tumor)ITGB3, NID1, FN1, FLNA, KDR, ITGAV, THBS1, ILK, PECAM1, DAB2, PDGFRB, CDCA8, CD36, TLN1, ANKS1B, TENC1, ITGB3BP, NFATC1, FBLN2, PDGFRA, ITGA5 (normal)
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THCA (tumor)THCA (normal)
ITGB3, FLNB, PTPN11, YES1, ITGAV, NFATC2, PTK2, ILK, EPS8, PECAM1, RABGAP1, CIB1, MAP3K13, TLN1, NUMB, ANKS1B, PDPK1, DOK1, GULP1, P2RY2, MYO10 (tumor)ITGB3, FLNA, PTPN1, PTPN11, LYN, YES1, ITGAV, NFATC2, PTK2, AKT1, EPS8, PECAM1, RABGAP1, TGM2, CIB1, MAP3K13, TLN1, CAPN1, PDPK1, P2RY2, THY1 (normal)
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TissGeneProg for ITGB3

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 ITGB3
TissGeneDrug for ITGB3

check button Drug information targeting TissGene
(DrugBank Version 5.0.6, 2017-04-01)
DrugBank IDDrug nameDrug activityDrug typeDrug status
DB00098Anti-thymocyte Globulin (Rabbit)BiotechApproved
DB00775TirofibanAntagonistSmall moleculeApproved
DB00063EptifibatideBiotechApproved|Investigational


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TissGeneDisease for ITGB3

check button Disease information associated with TissGene
(DisGeNet, 2016-06-01)
Disease IDDisease name# pubmedsSource
umls:C0040015Thrombasthenia46BeFree,CLINVAR,CTD_human,GAD,LHGDN,MGD,ORPHANET,UNIPROT
umls:C0027051Myocardial Infarction44BeFree,CLINVAR,CTD_human,GAD,LHGDN,RGD
umls:C0038454Cerebrovascular accident26BeFree,CTD_human,GAD,LHGDN,RGD
umls:C0010054Coronary Arteriosclerosis21BeFree,GAD
umls:C1956346Coronary Artery Disease19BeFree,GAD,LHGDN
umls:C0007222Cardiovascular Diseases16BeFree,GAD
umls:C0010068Coronary heart disease14BeFree,GAD
umls:C0010072Coronary Thrombosis11BeFree,CTD_human,GAD
umls:C0040053Thrombosis11GAD,LHGDN
umls:C0006142Malignant neoplasm of breast10BeFree,GAD
umls:C0027627Neoplasm Metastasis10BeFree,LHGDN
umls:C1458155Mammary Neoplasms10BeFree,LHGDN
umls:C0948089Acute Coronary Syndrome9BeFree,CTD_human,GAD,LHGDN
umls:C0004352Autistic Disorder8BeFree,CTD_human,GAD,LHGDN
umls:C0020538Hypertensive disease8BeFree,GAD
umls:C0333186Restenosis8BeFree,GAD
umls:C0004153Atherosclerosis7BeFree,GAD
umls:C0033578Prostatic Neoplasms7CTD_human,LHGDN
umls:C0398623Thrombophilia7BeFree,GAD
umls:C0678222Breast Carcinoma7BeFree
umls:C0004096Asthma6BeFree,GAD,LHGDN
umls:C0007786Brain Ischemia6GAD
umls:C0025202melanoma6BeFree,LHGDN
umls:C0151744Myocardial Ischemia6GAD
umls:C0155626Acute myocardial infarction6BeFree
umls:C0040034Thrombocytopenia5CTD_human,GAD,LHGDN
umls:C0948008Ischemic stroke5BeFree,GAD
umls:C1842372ASPIRIN RESISTANCE5GAD
umls:C0011860Diabetes Mellitus, Non-Insulin-Dependent4BeFree,GAD
umls:C0024314Lymphoproliferative Disorders4GAD
umls:C0040038Thromboembolism4BeFree,GAD
umls:C0242379Malignant neoplasm of lung4BeFree,GAD
umls:C0836924Thrombocytosis4BeFree
umls:C0001418Adenocarcinoma3BeFree,LHGDN
umls:C0003850Arteriosclerosis3BeFree,GAD
umls:C0009402Colorectal Carcinoma3BeFree
umls:C0018817Atrial Septal Defects3BeFree
umls:C0021368Inflammation3GAD
umls:C0023418leukemia3BeFree
umls:C0024141Lupus Erythematosus, Systemic3GAD,LHGDN
umls:C0029925Ovarian Carcinoma3BeFree
umls:C0035326Retinal vascular occlusion3GAD
umls:C0038525Subarachnoid Hemorrhage3BeFree,GAD,LHGDN
umls:C0042373Vascular Diseases3BeFree,GAD
umls:C0398650Immune thrombocytopenic purpura3BeFree,LHGDN
umls:C0687675Pregnancy loss3GAD
umls:C0919267ovarian neoplasm3LHGDN
umls:C0948201Alloimmunisation3BeFree
umls:C1140680Malignant neoplasm of ovary3BeFree,GAD
umls:C1264031Alloimmune thrombocytopenia3BeFree
umls:C1527249Colorectal Cancer3BeFree,GAD
umls:C3853779Neonatal Alloimmune Thrombocytopenia3CTD_human,GAD,LHGDN
umls:C0000786Spontaneous abortion2GAD,LHGDN
umls:C0000809Abortion, Habitual2GAD
umls:C0002895Anemia, Sickle Cell2GAD
umls:C0005818Blood Platelet Disorders2BeFree,GAD
umls:C0007131Non-Small Cell Lung Carcinoma2BeFree
umls:C0007787Transient Ischemic Attack2GAD,RGD
umls:C0011881Diabetic Nephropathy2BeFree
umls:C0017327Generalized atherosclerosis2GAD
umls:C0019080Hemorrhage2CTD_human,GAD
umls:C0019087Hemorrhagic Disorders2GAD
umls:C0019101Hemorrhagic Fever with Renal Syndrome2GAD,LHGDN
umls:C0019693HIV Infections2BeFree
umls:C0021361Female infertility2GAD
umls:C0021390Inflammatory Bowel Diseases2BeFree,GAD
umls:C0022661Kidney Failure, Chronic2GAD
umls:C0028754Obesity2GAD
umls:C0031117Peripheral Neuropathy2CTD_human,GAD
umls:C0032914Pre-Eclampsia2GAD
umls:C0040028Thrombocythemia, Essential2BeFree
umls:C0085096Peripheral Vascular Diseases2GAD
umls:C0085298Sudden Cardiac Death2GAD
umls:C0149931Migraine Disorders2GAD
umls:C0684249Carcinoma of lung2BeFree
umls:C0686619Secondary malignant neoplasm of lymph node2BeFree
umls:C0751633Carotid Artery Plaque2BeFree
umls:C1510586Autism Spectrum Disorders2BeFree
umls:C1561955Fibrinogen Adverse Event2GAD
umls:C1861172Venous Thromboembolism2GAD
umls:C1868251Neonatal alloimmune thrombocytopenia (NAIT)2BeFree
umls:C0001925Albuminuria1GAD
umls:C0002736Amyotrophic Lateral Sclerosis1GAD
umls:C0002874Aplastic Anemia1LHGDN
umls:C0002962Angina Pectoris1GAD
umls:C0002965Angina, Unstable1LHGDN
umls:C0003130Anoxia1LHGDN
umls:C0003838Arterial Occlusive Diseases1RGD
umls:C0003873Rheumatoid Arthritis1BeFree
umls:C0004238Atrial Fibrillation1GAD
umls:C0004626Pneumonia, Bacterial1RGD
umls:C0004936Mental disorders1BeFree
umls:C0004943Behcet Syndrome1BeFree
umls:C0005283beta Thalassemia1GAD
umls:C0007137Squamous cell carcinoma1GAD
umls:C0007273Carotid Artery Diseases1GAD
umls:C0007274Carotid Artery Thrombosis1CTD_human
umls:C0007282Carotid Stenosis1GAD
umls:C0007766Intracranial Aneurysm1GAD
umls:C0007772Intracranial Arteriovenous Malformation1LHGDN
umls:C0007789Cerebral Palsy1GAD
umls:C0007820Cerebrovascular Disorders1GAD
umls:C0008074Child Development Disorders, Pervasive1CTD_human
umls:C0008479Chondrosarcoma1LHGDN
umls:C0008495Chorioamnionitis1GAD
umls:C0008924Cleft Lip1BeFree
umls:C0009404Colorectal Neoplasms1GAD
umls:C0010346Crohn Disease1BeFree
umls:C0011057Hearing Loss, Sudden1GAD
umls:C0011644Scleroderma1BeFree
umls:C0011853Diabetes Mellitus, Experimental1RGD
umls:C0011854Diabetes Mellitus, Insulin-Dependent1BeFree
umls:C0011884Diabetic Retinopathy1BeFree
umls:C0014121Bacterial Endocarditis1BeFree
umls:C0014175Endometriosis1LHGDN
umls:C0014591Epistaxis1GAD
umls:C0015944Fetal Membranes, Premature Rupture1GAD
umls:C0015967Fever1LHGDN
umls:C0017181Gastrointestinal Hemorrhage1GAD
umls:C0017638Glioma1BeFree
umls:C0017639Gliosis1CTD_human
umls:C0017658Glomerulonephritis1RGD
umls:C0018128Graft Occlusion, Vascular1GAD
umls:C0018784Sensorineural Hearing Loss (disorder)1GAD
umls:C0018799Heart Diseases1GAD
umls:C0019061Hemolytic-Uremic Syndrome1GAD
umls:C0019100Severe Dengue1GAD
umls:C0019196Hepatitis C1GAD
umls:C0019829Hodgkin Disease1LHGDN
umls:C0020445Hypercholesterolemia, Familial1BeFree
umls:C0020473Hyperlipidemia1GAD
umls:C0020517Hypersensitivity1GAD
umls:C0020732Iatrogenic Disease1GAD
umls:C0021308Infarction1LHGDN
umls:C0021775Intermittent Claudication1GAD
umls:C0022658Kidney Diseases1GAD
umls:C0022876Premature Obstetric Labor1GAD
umls:C0023473Myeloid Leukemia, Chronic1BeFree
umls:C0024121Lung Neoplasms1LHGDN
umls:C0024305Lymphoma, Non-Hodgkin1BeFree,GAD
umls:C0024668Mammary Neoplasms, Experimental1RGD
umls:C0026269Mitral Valve Stenosis1GAD
umls:C0026640Mouth Neoplasms1GAD
umls:C0026764Multiple Myeloma1LHGDN
umls:C0029134Optic Neuritis1GAD,LHGDN
umls:C0029463Osteosarcoma1LHGDN
umls:C0030805Bullous pemphigoid1LHGDN
umls:C0030920Peptic Ulcer1GAD
umls:C0032460Polycystic Ovary Syndrome1GAD
umls:C0032963Pregnancy Complications, Cardiovascular1GAD
umls:C0032964Pregnancy Complications, Hematologic1GAD
umls:C0033027Preleukemia1BeFree
umls:C0035126Reperfusion Injury1RGD
umls:C0035302Retinal Artery Occlusion1GAD
umls:C0035328Retinal Vein Occlusion1GAD
umls:C0036220Kaposi Sarcoma1BeFree
umls:C0036341Schizophrenia1BeFree
umls:C0036421Systemic Scleroderma1BeFree
umls:C0039263Takayasu Arteritis1LHGDN
umls:C0039483Giant Cell Arteritis1BeFree,GAD,LHGDN
umls:C0040336Tobacco Use Disorder1GAD
umls:C0042345Varicosity1BeFree
umls:C0042755Virilism1GAD
umls:C0042974von Willebrand Disease1GAD
umls:C0043194Wiskott-Aldrich Syndrome1BeFree
umls:C0079487Helicobacter Infections1GAD
umls:C0079731B-Cell Lymphomas1BeFree
umls:C0079745Lymphoma, Large-Cell, Follicular1BeFree
umls:C0085110Severe Combined Immunodeficiency1BeFree
umls:C0085278Antiphospholipid Syndrome1GAD
umls:C0149871Deep Vein Thrombosis1BeFree
umls:C0151526Premature Birth1GAD
umls:C0151950Deep thrombophlebitis1BeFree
umls:C0152013Adenocarcinoma of lung (disorder)1BeFree
umls:C0155305Optic Neuropathy, Ischemic1GAD
umls:C0155668Old myocardial infarction1BeFree
umls:C0162869Aneurysm, Ruptured1GAD
umls:C0232197Fibrillation1BeFree
umls:C0242231Coronary Stenosis1BeFree
umls:C0242339Dyslipidemias1GAD
umls:C0242383Age related macular degeneration1GAD
umls:C0242584Autoimmune thrombocytopenia1BeFree
umls:C0264683Coronary artery atheroma1BeFree
umls:C0265808Cyanotic congenital heart disease1BeFree
umls:C0280141Acute Undifferentiated Leukemia1BeFree
umls:C0338656Impaired cognition1BeFree
umls:C0342257Complications of Diabetes Mellitus1GAD
umls:C0376358Malignant neoplasm of prostate1GAD
umls:C0376618Endotoxemia1RGD
umls:C0398356Abdominal aortic atherosclerosis1BeFree
umls:C0553692Brain hemorrhage1GAD
umls:C0577698Exercise-induced angina1BeFree
umls:C0596263Carcinogenesis1BeFree
umls:C0598608Hyperhomocysteinemia1GAD
umls:C0598766Leukemogenesis1BeFree
umls:C0598935Tumor Initiation1BeFree
umls:C0740457Malignant neoplasm of kidney1GAD
umls:C0741923cardiac event1BeFree
umls:C0750145vascular disease occlusive1BeFree
umls:C0750151Vaso-occlusive crisis1GAD
umls:C0751711Anterior Ischemic Optic Neuropathy1BeFree
umls:C0752140Intracranial Embolism1GAD
umls:C0752143Intracranial Thrombosis1GAD
umls:C0752351Embryo Loss1GAD
umls:C0852077Blood Coagulation Disorders, Inherited1GAD
umls:C0872054latent infection1BeFree
umls:C0993582Arthritis, Experimental1RGD
umls:C1272641Systemic arterial pressure1GAD
umls:C1273976First myocardial infarction1BeFree
umls:C1319200Postoperative confusion1BeFree
umls:C1378511Undifferentiated leukemia1BeFree
umls:C1541923Infective endocarditis1BeFree
umls:C1857941Brooke-Spiegler syndrome1BeFree
umls:C1861185THROMBOCYTOPENIA 2 (disorder)1BeFree
umls:C1861195Glanzmann Thrombasthenia, Autosomal Dominant1CLINVAR,MGD,UNIPROT
umls:C1956391Temporal Arteritis1GAD
umls:C2349404Heparin induced thrombocytopenia (HIT)1BeFree
umls:C2919032Infection of amniotic sac and membranes, unspecified, unspecified trimester, not applicable or unspecified1GAD
umls:C2921106Recurrent pregnancy loss1GAD
umls:C2937358Cerebral Hemorrhage1CTD_human
umls:C3178801Stroke, Lacunar1GAD
umls:C3272363Ischemic Cerebrovascular Accident1BeFree
umls:C3463824MYELODYSPLASTIC SYNDROME1BeFree
umls:C3539878Triple Negative Breast Neoplasms1BeFree
umls:C3539909Allergic disposition1BeFree
umls:C0398648Posttransfusion purpura0CLINVAR
umls:C2674640FRACTURE, HIP, SUSCEPTIBILITY TO (finding)0CLINVAR