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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:C3-ALB (FusionGDB2 ID:HG718TG213)

Fusion Gene Summary for C3-ALB

check button Fusion gene summary
Fusion gene informationFusion gene name: C3-ALB
Fusion gene ID: hg718tg213
HgeneTgene
Gene symbol

C3

ALB

Gene ID

718

213

Gene namecomplement C3albumin
SynonymsAHUS5|ARMD9|ASP|C3a|C3b|CPAMD1|HEL-S-62pHSA|PRO0883|PRO0903|PRO1341
Cytomap('C3')('ALB')

19p13.3

4q13.3

Type of geneprotein-codingprotein-coding
Descriptioncomplement C3C3 and PZP-like alpha-2-macroglobulin domain-containing protein 1C3a anaphylatoxinacylation-stimulating protein cleavage productcomplement component 3complement component C3acomplement component C3bepididymis secretory sperm binding prserum albumin
Modification date2020032720200329
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000245907, ENST00000599668, 
ENST00000245907, ENST00000599668, 
Fusion gene scores* DoF score28 X 24 X 14=940849 X 62 X 5=15190
# samples 3364
** MAII scorelog2(33/9408*10)=-4.83335013059055
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(64/15190*10)=-4.56890615450208
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: C3 [Title/Abstract] AND ALB [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointC3(6677874)-ALB(74283824), # samples:1
C3(6684574)-ALB(74285322), # samples:1
C3(6682029)-ALB(74270017), # samples:1
Anticipated loss of major functional domain due to fusion event.ALB-C3 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
ALB-C3 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
C3-ALB seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
C3-ALB seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
C3-ALB seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneC3

GO:0001934

positive regulation of protein phosphorylation

15833747

HgeneC3

GO:0010575

positive regulation of vascular endothelial growth factor production

16452172

HgeneC3

GO:0010828

positive regulation of glucose transmembrane transport

9059512|15833747

HgeneC3

GO:0010866

regulation of triglyceride biosynthetic process

10432298

HgeneC3

GO:0010884

positive regulation of lipid storage

9555951

HgeneC3

GO:0045745

positive regulation of G protein-coupled receptor signaling pathway

15833747

TgeneALB

GO:0009267

cellular response to starvation

16245148

TgeneALB

GO:0043066

negative regulation of apoptotic process

16153637

TgeneALB

GO:0051659

maintenance of mitochondrion location

16153637



check button Fusion gene information
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4CHOLTCGA-W5-AA30-11AC3chr19

6684574

-ALBchr4

74285322

+
ChimerDB4CHOLTCGA-ZU-A8S4-11AC3chr19

6677874

-ALBchr4

74283824

+


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Fusion Gene ORF analysis for C3-ALB

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
5CDS-3UTRENST00000245907ENST00000505649C3chr19

6684574

-ALBchr4

74285322

+
5CDS-3UTRENST00000599668ENST00000505649C3chr19

6677874

-ALBchr4

74283824

+
Frame-shiftENST00000245907ENST00000295897C3chr19

6684574

-ALBchr4

74285322

+
Frame-shiftENST00000245907ENST00000401494C3chr19

6684574

-ALBchr4

74285322

+
Frame-shiftENST00000245907ENST00000415165C3chr19

6684574

-ALBchr4

74285322

+
Frame-shiftENST00000245907ENST00000503124C3chr19

6684574

-ALBchr4

74285322

+
Frame-shiftENST00000245907ENST00000509063C3chr19

6684574

-ALBchr4

74285322

+
Frame-shiftENST00000599668ENST00000295897C3chr19

6677874

-ALBchr4

74283824

+
Frame-shiftENST00000599668ENST00000401494C3chr19

6677874

-ALBchr4

74283824

+
Frame-shiftENST00000599668ENST00000415165C3chr19

6677874

-ALBchr4

74283824

+
Frame-shiftENST00000599668ENST00000503124C3chr19

6677874

-ALBchr4

74283824

+
Frame-shiftENST00000599668ENST00000509063C3chr19

6677874

-ALBchr4

74283824

+
intron-3CDSENST00000245907ENST00000295897C3chr19

6677874

-ALBchr4

74283824

+
intron-3CDSENST00000245907ENST00000401494C3chr19

6677874

-ALBchr4

74283824

+
intron-3CDSENST00000245907ENST00000415165C3chr19

6677874

-ALBchr4

74283824

+
intron-3CDSENST00000245907ENST00000503124C3chr19

6677874

-ALBchr4

74283824

+
intron-3CDSENST00000245907ENST00000509063C3chr19

6677874

-ALBchr4

74283824

+
intron-3CDSENST00000599668ENST00000295897C3chr19

6684574

-ALBchr4

74285322

+
intron-3CDSENST00000599668ENST00000401494C3chr19

6684574

-ALBchr4

74285322

+
intron-3CDSENST00000599668ENST00000415165C3chr19

6684574

-ALBchr4

74285322

+
intron-3CDSENST00000599668ENST00000503124C3chr19

6684574

-ALBchr4

74285322

+
intron-3CDSENST00000599668ENST00000509063C3chr19

6684574

-ALBchr4

74285322

+
intron-3UTRENST00000245907ENST00000505649C3chr19

6677874

-ALBchr4

74283824

+
intron-3UTRENST00000599668ENST00000505649C3chr19

6684574

-ALBchr4

74285322

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)		BP loci
(transcript)		Predicted start
(transcript)		Predicted stop
(transcript)		Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for C3-ALB


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)


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Fusion Protein Features for C3-ALB


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:6677874/:74283824)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
..
FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page


* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for C3-ALB


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for C3-ALB


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for C3-ALB


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for C3-ALB


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneC3C3151071COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE5CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneC3C0242383Age related macular degeneration4CTD_human;GENOMICS_ENGLAND
HgeneC3C2752037HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 54GENOMICS_ENGLAND;UNIPROT
HgeneC3C1969651Macular Degeneration, Age-Related, 92CTD_human;UNIPROT
HgeneC3C0003257Antibody Deficiency Syndrome1CTD_human
HgeneC3C0007787Transient Ischemic Attack1CTD_human
HgeneC3C0011860Diabetes Mellitus, Non-Insulin-Dependent1CTD_human
HgeneC3C0013221Drug toxicity1CTD_human
HgeneC3C0017665Membranous glomerulonephritis1CTD_human
HgeneC3C0019061Hemolytic-Uremic Syndrome1GENOMICS_ENGLAND
HgeneC3C0019193Hepatitis, Toxic1CTD_human
HgeneC3C0021051Immunologic Deficiency Syndromes1CTD_human
HgeneC3C0021655Insulin Resistance1CTD_human
HgeneC3C0022660Kidney Failure, Acute1CTD_human
HgeneC3C0030524Paratuberculosis1CTD_human
HgeneC3C0030807Pemphigus1CTD_human
HgeneC3C0030809Pemphigus Vulgaris1CTD_human
HgeneC3C0034152Henoch-Schoenlein Purpura1CTD_human
HgeneC3C0041755Adverse reaction to drug1CTD_human
HgeneC3C0042386Vasculitis, Hemorrhagic1CTD_human
HgeneC3C0086445Idiopathic Membranous Glomerulonephritis1CTD_human
HgeneC3C0086922Rheumatoid Purpura1CTD_human
HgeneC3C0238281Middle Cerebral Artery Syndrome1CTD_human
HgeneC3C0242461Purpura, Nonthrombocytopenic1CTD_human
HgeneC3C0263313Pemphigus Foliaceus1CTD_human
HgeneC3C0272242Complement deficiency disease1GENOMICS_ENGLAND
HgeneC3C0376362Purpura Hemorrhagica1CTD_human
HgeneC3C0472381Posterior Circulation Transient Ischemic Attack1CTD_human
HgeneC3C0740376Middle Cerebral Artery Thrombosis1CTD_human
HgeneC3C0740391Middle Cerebral Artery Occlusion1CTD_human
HgeneC3C0740392Infarction, Middle Cerebral Artery1CTD_human
HgeneC3C0751019Carotid Circulation Transient Ischemic Attack1CTD_human
HgeneC3C0751020Transient Ischemic Attack, Vertebrobasilar Circulation1CTD_human
HgeneC3C0751021Crescendo Transient Ischemic Attacks1CTD_human
HgeneC3C0751022Brain Stem Ischemia, Transient1CTD_human
HgeneC3C0751845Middle Cerebral Artery Embolus1CTD_human
HgeneC3C0751846Left Middle Cerebral Artery Infarction1CTD_human
HgeneC3C0751847Embolic Infarction, Middle Cerebral Artery1CTD_human
HgeneC3C0751848Thrombotic Infarction, Middle Cerebral Artery1CTD_human
HgeneC3C0751849Right Middle Cerebral Artery Infarction1CTD_human
HgeneC3C0860207Drug-Induced Liver Disease1CTD_human
HgeneC3C0917805Transient Cerebral Ischemia1CTD_human
HgeneC3C0920563Insulin Sensitivity1CTD_human
HgeneC3C1262760Hepatitis, Drug-Induced1CTD_human
HgeneC3C1332655Complement component 3 deficiency1GENOMICS_ENGLAND
HgeneC3C1527335Transient Ischemic Attack, Anterior Circulation1CTD_human
HgeneC3C1565662Acute Kidney Insufficiency1CTD_human
HgeneC3C1704378Heymann Nephritis1CTD_human
HgeneC3C2609414Acute kidney injury1CTD_human
HgeneC3C2931788Atypical Hemolytic Uremic Syndrome1CTD_human;GENOMICS_ENGLAND
HgeneC3C3658290Drug-Induced Acute Liver Injury1CTD_human
HgeneC3C4087273C3 glomerulopathy1GENOMICS_ENGLAND
HgeneC3C4277682Chemical and Drug Induced Liver Injury1CTD_human
HgeneC3C4279912Chemically-Induced Liver Toxicity1CTD_human
TgeneC0033687Proteinuria9CTD_human
TgeneC0017658Glomerulonephritis8CTD_human
TgeneC0022658Kidney Diseases8CTD_human
TgeneC1704377Bright Disease8CTD_human
TgeneC0017665Membranous glomerulonephritis6CTD_human
TgeneC0027697Nephritis6CTD_human
TgeneC0086445Idiopathic Membranous Glomerulonephritis6CTD_human
TgeneC0342185Hyperthyroxinemia, Familial Dysalbuminemic6CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneC1704378Heymann Nephritis6CTD_human
TgeneC0022660Kidney Failure, Acute4CTD_human
TgeneC0027707Nephritis, Interstitial4CTD_human
TgeneC0038454Cerebrovascular accident4CTD_human
TgeneC0041349Nephritis, Tubulointerstitial4CTD_human
TgeneC0751956Acute Cerebrovascular Accidents4CTD_human
TgeneC1565662Acute Kidney Insufficiency4CTD_human
TgeneC2609414Acute kidney injury4CTD_human
TgeneC0023893Liver Cirrhosis, Experimental3CTD_human
TgeneC0025290Aseptic Meningitis3CTD_human
TgeneC0013221Drug toxicity2CTD_human
TgeneC0014544Epilepsy2CTD_human
TgeneC0019193Hepatitis, Toxic2CTD_human
TgeneC0020649Hypotension2CTD_human
TgeneC0023890Liver Cirrhosis2CTD_human
TgeneC0027726Nephrotic Syndrome2CTD_human
TgeneC0036830Serum Sickness2CTD_human
TgeneC0041755Adverse reaction to drug2CTD_human
TgeneC0086237Epilepsy, Cryptogenic2CTD_human
TgeneC0162557Liver Failure, Acute2CTD_human
TgeneC0236018Aura2CTD_human
TgeneC0239946Fibrosis, Liver2CTD_human
TgeneC0751111Awakening Epilepsy2CTD_human
TgeneC0860207Drug-Induced Liver Disease2CTD_human
TgeneC0878666Analbuminemia2ORPHANET
TgeneC1262760Hepatitis, Drug-Induced2CTD_human
TgeneC3658290Drug-Induced Acute Liver Injury2CTD_human
TgeneC4277682Chemical and Drug Induced Liver Injury2CTD_human
TgeneC4279912Chemically-Induced Liver Toxicity2CTD_human
TgeneC0002994Angioedema1CTD_human
TgeneC0003460Anuria1CTD_human
TgeneC0003865Arthritis, Adjuvant-Induced1CTD_human
TgeneC0004509Azoospermia1CTD_human
TgeneC0005398Cholestasis, Extrahepatic1CTD_human
TgeneC0006111Brain Diseases1CTD_human
TgeneC0007222Cardiovascular Diseases1CTD_human
TgeneC0007786Brain Ischemia1CTD_human
TgeneC0008312Primary biliary cirrhosis1CTD_human
TgeneC0011573Endogenous depression1CTD_human
TgeneC0011581Depressive disorder1CTD_human
TgeneC0011875Diabetic Angiopathies1CTD_human
TgeneC0011881Diabetic Nephropathy1CTD_human
TgeneC0013502Echinococcosis1CTD_human
TgeneC0014518Toxic Epidermal Necrolysis1CTD_human
TgeneC0016059Fibrosis1CTD_human
TgeneC0017662Glomerulonephritis, Membranoproliferative1CTD_human
TgeneC0017667Nodular glomerulosclerosis1CTD_human
TgeneC0018799Heart Diseases1CTD_human
TgeneC0018801Heart failure1CTD_human
TgeneC0018802Congestive heart failure1CTD_human
TgeneC0019061Hemolytic-Uremic Syndrome1CTD_human
TgeneC0019158Hepatitis1CTD_human
TgeneC0019209Hepatomegaly1CTD_human
TgeneC0019693HIV Infections1CTD_human
TgeneC0019699HIV Seropositivity1CTD_human
TgeneC0020517Hypersensitivity1CTD_human
TgeneC0020522Delayed Hypersensitivity1CTD_human
TgeneC0020538Hypertensive disease1CTD_human
TgeneC0022548Keloid1CTD_human
TgeneC0022661Kidney Failure, Chronic1CTD_human
TgeneC0023212Left-Sided Heart Failure1CTD_human
TgeneC0023892Biliary cirrhosis1CTD_human
TgeneC0024623Malignant neoplasm of stomach1CTD_human
TgeneC0025193Melancholia1CTD_human
TgeneC0025945Microangiopathy, Diabetic1CTD_human
TgeneC0026848Myopathy1CTD_human
TgeneC0027055Myocardial Reperfusion Injury1CTD_human
TgeneC0027720Nephrosis1CTD_human
TgeneC0028797Occupational Diseases1CTD_human
TgeneC0030193Pain1CTD_human
TgeneC0030286Pancreatic Diseases1CTD_human
TgeneC0030305Pancreatitis1CTD_human
TgeneC0035222Respiratory Distress Syndrome, Adult1CTD_human
TgeneC0035242Respiratory Tract Diseases1CTD_human
TgeneC0035457Rhinitis, Allergic, Perennial1CTD_human
TgeneC0038325Stevens-Johnson Syndrome1CTD_human
TgeneC0038356Stomach Neoplasms1CTD_human
TgeneC0040034Thrombocytopenia1CTD_human
TgeneC0041696Unipolar Depression1CTD_human
TgeneC0042109Urticaria1CTD_human
TgeneC0042164Uveitis1CTD_human
TgeneC0085584Encephalopathies1CTD_human
TgeneC0086133Depressive Syndrome1CTD_human
TgeneC0152013Adenocarcinoma of lung (disorder)1CTD_human
TgeneC0234230Pain, Burning1CTD_human
TgeneC0234238Ache1CTD_human
TgeneC0234254Radiating pain1CTD_human
TgeneC0235527Heart Failure, Right-Sided1CTD_human
TgeneC0238065Secondary Biliary Cholangitis1CTD_human
TgeneC0239981Hypoalbuminemia1CTD_human
TgeneC0268742Membranoproliferative Glomerulonephritis, Type I1CTD_human
TgeneC0268743Membranoproliferative Glomerulonephritis, Type II1CTD_human
TgeneC0273115Lung Injury1CTD_human
TgeneC0282126Depression, Neurotic1CTD_human
TgeneC0458257Pain, Splitting1CTD_human
TgeneC0458259Pain, Crushing1CTD_human
TgeneC0751407Pain, Migratory1CTD_human
TgeneC0751408Suffering, Physical1CTD_human
TgeneC0917798Cerebral Ischemia1CTD_human
TgeneC0971858Arthritis, Collagen-Induced1CTD_human
TgeneC0993582Arthritis, Experimental1CTD_human
TgeneC1274933Drug-Induced Stevens Johnson Syndrome1CTD_human
TgeneC1306571Hepatic Insufficiency1CTD_human
TgeneC1527304Allergic Reaction1CTD_human
TgeneC1623038Cirrhosis1CTD_human
TgeneC1708349Hereditary Diffuse Gastric Cancer1CTD_human
TgeneC1720821Membranoproliferative Glomerulonephritis, Type III1CTD_human
TgeneC1959583Myocardial Failure1CTD_human
TgeneC1961112Heart Decompensation1CTD_human
TgeneC2350344Chronic Lung Injury1CTD_human
TgeneC3658301Mycoplasma-Induced Stevens-Johnson Syndrome1CTD_human
TgeneC3658302Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum1CTD_human
TgeneC4505456HIV Coinfection1CTD_human
TgeneC4551595Biliary Cirrhosis, Primary, 11CTD_human
TgeneC4553297Cystic Echinocccosis1CTD_human