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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 CYP2C9
check button Gene summary
Basic gene informationGene symbolCYP2C9
Gene namecytochrome P450, family 2, subfamily C, polypeptide 9
SynonymsCPC9|CYP2C|CYP2C10|CYPIIC9|P450IIC9
CytomapUCSC genome browser: 10q24
Type of geneprotein-coding
RefGenesNM_000771.3,
Descriptioncytochrome P-450 S-mephenytoin 4-hydroxylasecytochrome P-450MPcytochrome P450 2C9cytochrome P450 PB-1flavoprotein-linked monooxygenasemicrosomal monooxygenasexenobiotic monooxygenase
Modification date20141211
dbXrefs MIM : 601130
HGNC : HGNC
Ensembl : ENSG00000138109
HPRD : 03084
Vega : OTTHUMG00000018805
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_CYP2C9
BioGPS: 1559
PathwayNCI Pathway Interaction Database: CYP2C9
KEGG: CYP2C9
REACTOME: CYP2C9
Pathway Commons: CYP2C9
ContextiHOP: CYP2C9
ligand binding site mutation search in PubMed: CYP2C9
UCL Cancer Institute: CYP2C9
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 CYP2C9High expression of the mRNA of cytochrome P450 and phase II enzymes in the lung and kidney tissues of cattle. Darwish WS, Ikenaka Y, El-Ghareeb WR, Ishizuka M. Animal. 2010 Dec;4(12):2023-9. doi: 10.1017/S1751731110001394. (pmid:22445377)
go to article
Description by TissGene annotationsCancer gene
* 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:0016098monoterpenoid metabolic process16401082
GO:0017144drug metabolic process19219744
GO:0019627urea metabolic process19029318
GO:0032787monocarboxylic acid metabolic process19651758
GO:0042738exogenous drug catabolic process18619574
GO:0043603cellular amide metabolic process19651758
GO:0055114oxidation-reduction process16401082
GO:0070989oxidative demethylation18619574
GO:0016098monoterpenoid metabolic process16401082
GO:0017144drug metabolic process19219744
GO:0019627urea metabolic process19029318
GO:0032787monocarboxylic acid metabolic process19651758
GO:0042738exogenous drug catabolic process18619574
GO:0043603cellular amide metabolic process19651758
GO:0055114oxidation-reduction process16401082
GO:0070989oxidative demethylation18619574


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TissGeneExp for CYP2C9

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-2.2158633680.822528632-3.0383924.94E-124.99E-11
LIHC9.52678863212.85690263-3.3301142.30E-124.19E-11
HNSC-0.3228700661.087225283-1.4100953490.0004270.00162839


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TissGene-miRNA for CYP2C9

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 CYP2C9
TissGeneSNV for CYP2C9

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.E199KSKCM3
p.E85KSKCM2
p.P363SSKCM2
p.E250KSKCM2
p.S390FSKCM2
p.M269ISKCM2
p.R357TCESC1
p.R329HLGG1
p.I88TTHCA1
p.G437ESKCM1
p.R335QUCEC1
p.M129ICESC1
p.S220FSKCM1
p.R186CBLCA1
p.E246KSKCM1
p.M255ISKCM1
p.T301MPRAD1
p.L362FCESC1
p.L152FSKCM1
p.L19ILGG1
p.P37SSKCM1
p.P279SSKCM1
p.D188HBLCA1
p.Q454HREAD1
p.Q484XKICH1
p.G135RSKCM1
p.R335WDLBC1
p.Y243HSKCM1
p.S286ISARC1
p.I331FLUAD1
p.G417SSKCM1
p.G109RLUAD1
p.R26SSKCM1
p.P404TLUSC1
p.A103VLUAD1
p.W212*SKCM1
p.E93KHNSC1
p.Q252PUCS1
p.D256NSKCM1
p.Y61HPRAD1
p.R108TSKCM1
p.S460YUCEC1
p.M198ISKCM1
p.I389TLUSC1
p.P367SSKCM1
p.E354KSKCM1
p.S336IESCA1
p.P174TESCA1
p.P402SLUAD1
p.R139KSKCM1
p.M1ISKCM1
p.K383*SKCM1
p.G109RSKCM1
p.P166LSKCM1
p.P279LSKCM1
p.L458VBRCA1
p.D468HESCA1
p.P35LSKCM1
p.G117ESKCM1
p.T364ISKCM1
p.A309SSKCM1
p.T130MBLCA1
p.E122KSKCM1
p.S127FSKCM1
p.Q252*SKCM1
p.W212XSKCM1
p.K138NHNSC1
p.D414NSKCM1
p.G442DPAAD1
p.M443ISKCM1
p.D188NSKCM1
p.R335QSKCM1
p.L413MLIHC1
p.S12LSKCM1
p.R124QLUAD1
p.A149THNSC1
p.L195FSKCM1
p.R335QSARC1
p.P30SHNSC1
p.Q252HLUAD1
p.E285KSKCM1
p.Q324*SKCM1
p.R125CPRAD1
p.V237ISTAD1
p.G135VESCA1
p.E199DREAD1
p.I264VLIHC1
p.D463YLUAD1
p.L19FSKCM1
p.I47VESCA1
p.G27ESKCM1
p.R186HPAAD1
p.R433WREAD1
p.K185TREAD1
p.G79ELGG1
p.V38ASKCM1
p.P489LSKCM1
p.C164RLIHC1
p.E253KHNSC1
p.E328KBRCA1
p.D341YREAD1
p.G431ESKCM1
p.L90VLUSC1
p.L14SCOAD1
p.P402SSKCM1
p.L467IUCEC1
p.L11FSKCM1
p.G27EUCEC1
p.G117RSKCM1
p.P404SSKCM1
p.V323FLUAD1
p.E444DOV1


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TissGeneCNV for CYP2C9

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 CYP2C9

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
Chimerdb3.0ChiTaRsNAAV652799SMG1-CYP2C9chr16:18856881chr10:96740952


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TissGeneNet for CYP2C9

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)
CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (tumor)CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (normal)
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COAD (tumor)COAD (normal)
CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (tumor)CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (normal)
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HNSC (tumor)HNSC (normal)
CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (tumor)CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (normal)
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KICH (tumor)KICH (normal)
CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (tumor)CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (normal)
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KIRC (tumor)KIRC (normal)
CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (tumor)CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (normal)
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KIRP (tumor)KIRP (normal)
CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (tumor)CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (normal)
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LIHC (tumor)LIHC (normal)
CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (tumor)CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (normal)
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LUAD (tumor)LUAD (normal)
CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (tumor)CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (normal)
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LUSC (tumor)LUSC (normal)
CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (tumor)CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (normal)
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PRAD (tumor)PRAD (normal)
CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (tumor)CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (normal)
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STAD (tumor)STAD (normal)
CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (tumor)CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (normal)
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THCA (tumor)THCA (normal)
CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (tumor)CYP2C9, NR3C1, HNF4A, RXRA, MAST1, CDC37, NR1I2, RNF32, STAMBP, STAT5A, POR, NR1I3, RAB3D (normal)
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TissGeneProg for CYP2C9

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 CYP2C9
TissGeneDrug for CYP2C9

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 CYP2C9

check button Disease information associated with TissGene
(DisGeNet, 2016-06-01)
Disease IDDisease name# pubmedsSource
umls:C2608079WARFARIN SENSITIVITY (disorder)33BeFree,GAD
umls:C0014544Epilepsy22BeFree,GAD
umls:C1527249Colorectal Cancer22BeFree,GAD
umls:C0009402Colorectal Carcinoma14BeFree
umls:C0006142Malignant neoplasm of breast13BeFree,GAD
umls:C0011860Diabetes Mellitus, Non-Insulin-Dependent13BeFree,GAD
umls:C0019080Hemorrhage13CTD_human,GAD,LHGDN
umls:C0040038Thromboembolism9BeFree,GAD
umls:C0040053Thrombosis9GAD
umls:C0007222Cardiovascular Diseases8GAD
umls:C0020615Hypoglycemia8BeFree,GAD
umls:C0017181Gastrointestinal Hemorrhage7GAD
umls:C0020538Hypertensive disease7BeFree,GAD,LHGDN
umls:C0027051Myocardial Infarction7BeFree,GAD,LHGDN
umls:C0242379Malignant neoplasm of lung7BeFree,GAD
umls:C0005779Blood Coagulation Disorders5GAD
umls:C0009404Colorectal Neoplasms5GAD,LHGDN
umls:C0023895Liver diseases5BeFree,GAD
umls:C0678222Breast Carcinoma5BeFree
umls:C0860207Drug-Induced Liver Injury5CTD_human,GAD
umls:C1302401Adenoma of large intestine5BeFree
umls:C1956346Coronary Artery Disease5BeFree,GAD
umls:C2239176Liver carcinoma5BeFree
umls:C0001430Adenoma4BeFree,GAD
umls:C0011570Mental Depression4BeFree,GAD
umls:C0018799Heart Diseases4BeFree,GAD
umls:C0030920Peptic Ulcer4BeFree,GAD
umls:C0034065Pulmonary Embolism4BeFree,GAD
umls:C0149871Deep Vein Thrombosis4BeFree,GAD
umls:C1458155Mammary Neoplasms4BeFree,GAD
umls:C0004153Atherosclerosis3BeFree,GAD,LHGDN
umls:C0005684Malignant neoplasm of urinary bladder3GAD
umls:C0010054Coronary Arteriosclerosis3BeFree
umls:C0011849Diabetes Mellitus3BeFree,LHGDN
umls:C0013182Drug Allergy3CTD_human,GAD
umls:C0014859Esophageal Neoplasms3BeFree,GAD
umls:C0020473Hyperlipidemia3BeFree,GAD
umls:C0023434Chronic Lymphocytic Leukemia3BeFree,GAD
umls:C0024305Lymphoma, Non-Hodgkin3BeFree,GAD
umls:C0036572Seizures3BeFree,GAD
umls:C0041696Unipolar Depression3BeFree
umls:C0042487Venous Thrombosis3GAD
umls:C0085580Essential Hypertension3BeFree
umls:C0232197Fibrillation3BeFree
umls:C0546837Malignant neoplasm of esophagus3BeFree,GAD
umls:C0684249Carcinoma of lung3BeFree
umls:C0850666Helicobacter pylori infection3BeFree,GAD
umls:C0948008Ischemic stroke3BeFree
umls:C0948089Acute Coronary Syndrome3GAD
umls:C1269683Major Depressive Disorder3BeFree,GAD
umls:C1272641Systemic arterial pressure3GAD
umls:C3272363Ischemic Cerebrovascular Accident3BeFree
umls:C0003850Arteriosclerosis2BeFree
umls:C0003873Rheumatoid Arthritis2GAD
umls:C0004238Atrial Fibrillation2GAD
umls:C0011847Diabetes2BeFree
umls:C0018671Head and Neck Neoplasms2GAD
umls:C0019693HIV Infections2BeFree,GAD
umls:C0020443Hypercholesterolemia2GAD
umls:C0023055Laryngeal neoplasm2GAD
umls:C0023903Liver neoplasms2BeFree
umls:C0026640Mouth Neoplasms2GAD
umls:C0028754Obesity2BeFree,GAD
umls:C0030193Pain2BeFree
umls:C0031347Pharyngeal Neoplasms2GAD
umls:C0038354Stomach Diseases2BeFree
umls:C0038358Gastric ulcer2BeFree,GAD
umls:C0038454Cerebrovascular accident2BeFree,GAD
umls:C0038644Sudden infant death syndrome2BeFree
umls:C0041755Adverse reaction to drug2CTD_human
umls:C0042373Vascular Diseases2BeFree
umls:C0266807Acute gastrointestinal hemorrhage2BeFree
umls:C0278996Cancer of Head and Neck2BeFree
umls:C0279626Squamous cell carcinoma of esophagus2BeFree
umls:C0596263Carcinogenesis2BeFree
umls:C0750384Coumarin Resistance2BeFree,CTD_human
umls:C1168401Squamous cell carcinoma of the head and neck2BeFree
umls:C1861172Venous Thromboembolism2GAD
umls:C2675747Coumarin Sensitivity2BeFree,GAD
umls:C0002895Anemia, Sickle Cell1BeFree
umls:C0003864Arthritis1GAD
umls:C0004096Asthma1GAD
umls:C0006118Brain Neoplasms1BeFree,CTD_human
umls:C0007102Malignant tumor of colon1BeFree
umls:C0009181Cocarcinogenesis1GAD
umls:C0009375Colonic Neoplasms1GAD
umls:C0009952Febrile Convulsions1BeFree
umls:C0010068Coronary heart disease1BeFree
umls:C0011581Depressive disorder1BeFree
umls:C0011991Diarrhea1GAD
umls:C0013146Drug abuse1BeFree
umls:C0013336Dwarfism1BeFree
umls:C0014547Epilepsies, Partial1GAD
umls:C0017178Gastrointestinal Diseases1GAD
umls:C0017566Gingival Hyperplasia1GAD
umls:C0018801Heart failure1GAD
umls:C0018939Hematological Disease1GAD
umls:C0019193Hepatitis, Toxic1GAD
umls:C0019829Hodgkin Disease1BeFree,GAD
umls:C0020544Renal hypertension1GAD
umls:C0022116Ischemia1GAD
umls:C0022658Kidney Diseases1BeFree
umls:C0022661Kidney Failure, Chronic1GAD
umls:C0024115Lung diseases1BeFree
umls:C0024121Lung Neoplasms1LHGDN
umls:C0024143Lupus Nephritis1GAD
umls:C0024301Lymphoma, Follicular1GAD
umls:C0024623Malignant neoplasm of stomach1GAD
umls:C0026764Multiple Myeloma1BeFree,GAD
umls:C0026848Myopathy1GAD
umls:C0027497Nausea1GAD
umls:C0027658Neoplasms, Germ Cell and Embryonal1GAD
umls:C0027707Nephritis, Interstitial1CTD_human
umls:C0027765nervous system disorder1CTD_human
umls:C0027947Neutropenia1GAD
umls:C0029408Degenerative polyarthritis1GAD
umls:C0030922Peptic Ulcer Hemorrhage1CTD_human,GAD
umls:C0031099Periodontitis1GAD
umls:C0032460Polycystic Ovary Syndrome1GAD
umls:C0033687Proteinuria1GAD
umls:C0033774Pruritus1GAD
umls:C0035309Retinal Diseases1BeFree
umls:C0035457Rhinitis, Allergic, Perennial1GAD
umls:C0036421Systemic Scleroderma1GAD
umls:C0040034Thrombocytopenia1GAD
umls:C0040156Thyrotoxicosis1BeFree
umls:C0041327Tuberculosis, Pulmonary1GAD
umls:C0042963Vomiting1GAD
umls:C0079487Helicobacter Infections1GAD
umls:C0079772T-Cell Lymphoma1GAD
umls:C0085215Ovarian Failure, Premature1GAD
umls:C0085278Antiphospholipid Syndrome1GAD
umls:C0151744Myocardial Ischemia1BeFree
umls:C0151945Thrombosis of cerebral veins1BeFree
umls:C0152018Esophageal carcinoma1BeFree
umls:C0152097Disease of diaphragm1BeFree
umls:C0152171Idiopathic pulmonary hypertension1BeFree
umls:C0155668Old myocardial infarction1BeFree
umls:C0162429Malnutrition1BeFree,GAD
umls:C0206139Lichen Planus, Oral1BeFree,GAD
umls:C0235032Neurotoxicity Syndromes1GAD
umls:C0241910Hepatitis, Autoimmune1BeFree
umls:C0242510Drug usage1BeFree
umls:C0242992Multiple Chemical Sensitivity1GAD
umls:C0270736Essential Tremor1BeFree,GAD,LHGDN
umls:C0333641Atrophic1GAD
umls:C0340708Deep vein thrombosis of lower limb1BeFree
umls:C0345904Malignant neoplasm of liver1GAD
umls:C0376634Craniofacial Abnormalities1BeFree
umls:C0391957idiopathic epilepsy1BeFree
umls:C0398623Thrombophilia1GAD
umls:C0400966Non-alcoholic Fatty Liver Disease1BeFree
umls:C0524910Hepatitis C, Chronic1BeFree
umls:C0677886Epithelial ovarian cancer1GAD
umls:C0699790Colon Carcinoma1BeFree
umls:C0751956Acute Cerebrovascular Accidents1BeFree
umls:C0850572Adenomatous polyp of colon1BeFree
umls:C0852077Blood Coagulation Disorders, Inherited1GAD
umls:C0856761Budd-Chiari Syndrome1GAD
umls:C0878544Cardiomyopathies1CTD_human
umls:C0919267ovarian neoplasm1GAD
umls:C0920269Microsatellite Instability1GAD
umls:C1271104Blood pressure finding1GAD
umls:C1319853Asthma, Aspirin-Induced1BeFree
umls:C1519670Tumor Angiogenesis1BeFree
umls:C1565489Renal Insufficiency1GAD
umls:C1962972Proteinuria Adverse Event1GAD
umls:C2609414Acute kidney injury1CTD_human
umls:C2973725Pulmonary arterial hypertension1BeFree
umls:C3714844Pulmonary Hypertension, Primary, 1, With Hereditary Hemorrhagic Telangiectasia1BeFree