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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   laryngeal carcinoma
  

Disease ID 1729
Disease laryngeal carcinoma
Definition
A carcinoma of the larynx. [HPO:probinson]
Synonym
carcinoma laryngeal
carcinoma larynx
carcinoma of larynx
carcinoma of larynx (disorder)
carcinoma of the larynx
larnyx carcinoma
larynx carcinoma
DOID
UMLS
C0595989
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:12)
C0280324  |  squamous cell carcinoma of the larynx  |  19
C0007137  |  squamous cell carcinoma  |  19
C0007115  |  thyroid ca  |  2
C0007137  |  epidermoid carcinoma  |  1
C0238301  |  nasopharyngeal carcinoma  |  1
C0024205  |  lymphadenitis  |  1
C0023269  |  leiomyosarcoma  |  1
C0149925  |  small cell carcinoma  |  1
C0149642  |  cervical lymphadenitis  |  1
C0280324  |  epidermoid carcinoma of the larynx  |  1
C0153676  |  lung metastasis  |  1
C0006840  |  candidiasis  |  1
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:180)
176  |  ACAN  |  1.973  |  DISEASES
60  |  ACTB  |  1.886  |  DISEASES
8038  |  ADAM12  |  1.417  |  DISEASES
80332  |  ADAM33  |  1.469  |  DISEASES
9507  |  ADAMTS4  |  1.091  |  DISEASES
79026  |  AHNAK  |  2.377  |  DISEASES
113146  |  AHNAK2  |  2.272  |  DISEASES
283  |  ANG  |  2.398  |  DISEASES
8905  |  AP1S2  |  2.338  |  DISEASES
317  |  APAF1  |  1.343  |  DISEASES
8539  |  API5  |  1.305  |  DISEASES
50807  |  ASAP1  |  2.431  |  DISEASES
9334  |  B4GALT5  |  1.408  |  DISEASES
573  |  BAG1  |  1.293  |  DISEASES
596  |  BCL2  |  1.518  |  DISEASES
90427  |  BMF  |  1.091  |  DISEASES
648  |  BMI1  |  2.767  |  DISEASES
664  |  BNIP3  |  1.061  |  DISEASES
25855  |  BRMS1  |  2.317  |  DISEASES
682  |  BSG  |  1.853  |  DISEASES
768  |  CA9  |  2.287  |  DISEASES
285782  |  CAGE1  |  1.979  |  DISEASES
157922  |  CAMSAP1  |  2.82  |  DISEASES
11132  |  CAPN10  |  1.112  |  DISEASES
841  |  CASP8  |  1.456  |  DISEASES
842  |  CASP9  |  2.25  |  DISEASES
857  |  CAV1  |  1.709  |  DISEASES
100507056  |  CCAT1  |  1.073  |  DISEASES
6364  |  CCL20  |  1.121  |  DISEASES
896  |  CCND3  |  1.283  |  DISEASES
1233  |  CCR4  |  1.012  |  DISEASES
1235  |  CCR6  |  2.39  |  DISEASES
4345  |  CD200  |  1.178  |  DISEASES
960  |  CD44  |  2.691  |  DISEASES
961  |  CD47  |  1.032  |  DISEASES
923  |  CD6  |  2.576  |  DISEASES
9308  |  CD83  |  1.515  |  DISEASES
1024  |  CDK8  |  1.882  |  DISEASES
1029  |  CDKN2A  |  3.77  |  DISEASES
55165  |  CEP55  |  1.35  |  DISEASES
55743  |  CHFR  |  2.188  |  DISEASES
1164  |  CKS2  |  1.185  |  DISEASES
123920  |  CMTM3  |  1.969  |  DISEASES
10987  |  COPS5  |  2.077  |  DISEASES
1496  |  CTNNA2  |  1.308  |  DISEASES
1499  |  CTNNB1  |  2.454  |  DISEASES
2017  |  CTTN  |  1.9  |  DISEASES
1543  |  CYP1A1  |  1.888  |  DISEASES
1565  |  CYP2D6  |  1.52  |  DISEASES
1612  |  DAPK1  |  1.428  |  DISEASES
729582  |  DIRC3  |  2.315  |  DISEASES
1786  |  DNMT1  |  1.237  |  DISEASES
1791  |  DNTT  |  1.313  |  DISEASES
1893  |  ECM1  |  2.511  |  DISEASES
1977  |  EIF4E  |  2.859  |  DISEASES
1981  |  EIF4G1  |  1.462  |  DISEASES
1994  |  ELAVL1  |  2.186  |  DISEASES
2022  |  ENG  |  3.675  |  DISEASES
957  |  ENTPD5  |  1.466  |  DISEASES
2113  |  ETS1  |  1.655  |  DISEASES
7430  |  EZR  |  1.641  |  DISEASES
2272  |  FHIT  |  2.642  |  DISEASES
2305  |  FOXM1  |  1.631  |  DISEASES
50943  |  FOXP3  |  1.089  |  DISEASES
6624  |  FSCN1  |  1.786  |  DISEASES
23464  |  GCAT  |  1.51  |  DISEASES
11245  |  GPR176  |  1.899  |  DISEASES
2948  |  GSTM4  |  1.692  |  DISEASES
2950  |  GSTP1  |  1.205  |  DISEASES
10456  |  HAX1  |  1.526  |  DISEASES
3039  |  HBA1  |  1.647  |  DISEASES
3091  |  HIF1A  |  2.675  |  DISEASES
8091  |  HMGA2  |  1.347  |  DISEASES
100124700  |  HOTAIR  |  2.104  |  DISEASES
3262  |  HPVC1  |  3.047  |  DISEASES
3326  |  HSP90AB1  |  1.544  |  DISEASES
10553  |  HTATIP2  |  2.019  |  DISEASES
3451  |  IFNA17  |  2.033  |  DISEASES
3440  |  IFNA2  |  1.268  |  DISEASES
3664  |  IRF6  |  1.15  |  DISEASES
8516  |  ITGA8  |  1.675  |  DISEASES
3709  |  ITPR2  |  1.179  |  DISEASES
3725  |  JUN  |  1.041  |  DISEASES
9928  |  KIF14  |  2.179  |  DISEASES
3796  |  KIF2A  |  1.759  |  DISEASES
688  |  KLF5  |  1.446  |  DISEASES
3880  |  KRT19  |  1.903  |  DISEASES
3851  |  KRT4  |  1.11  |  DISEASES
84648  |  LCE3D  |  2.274  |  DISEASES
440556  |  LINC00982  |  2.639  |  DISEASES
101928555  |  LINC01537  |  1.877  |  DISEASES
4110  |  MAGEA11  |  1.536  |  DISEASES
57134  |  MAN1C1  |  1.15  |  DISEASES
5602  |  MAPK10  |  2.036  |  DISEASES
4193  |  MDM2  |  2.16  |  DISEASES
4237  |  MFAP2  |  1.396  |  DISEASES
100507436  |  MICA  |  1.256  |  DISEASES
554202  |  MIR31HG  |  1.877  |  DISEASES
4288  |  MKI67  |  1.121  |  DISEASES
4312  |  MMP1  |  1.811  |  DISEASES
4318  |  MMP9  |  2.775  |  DISEASES
9112  |  MTA1  |  1.365  |  DISEASES
92140  |  MTDH  |  2.427  |  DISEASES
2475  |  MTOR  |  1.311  |  DISEASES
100463285  |  MTRNR2L4  |  2.174  |  DISEASES
4604  |  MYBPC1  |  1.68  |  DISEASES
4609  |  MYC  |  2.795  |  DISEASES
80177  |  MYCT1  |  3.048  |  DISEASES
64859  |  NABP1  |  2.464  |  DISEASES
57446  |  NDRG3  |  1.852  |  DISEASES
51701  |  NLK  |  1.358  |  DISEASES
4831  |  NME2  |  2.364  |  DISEASES
283820  |  NOMO2  |  1.15  |  DISEASES
408050  |  NOMO3  |  1.152  |  DISEASES
152559  |  PAQR3  |  1.686  |  DISEASES
11315  |  PARK7  |  2.501  |  DISEASES
27253  |  PCDH17  |  1.659  |  DISEASES
9141  |  PDCD5  |  1.009  |  DISEASES
5203  |  PFDN4  |  1.383  |  DISEASES
80012  |  PHC3  |  2.605  |  DISEASES
51230  |  PHF20  |  1.164  |  DISEASES
57661  |  PHRF1  |  2.18  |  DISEASES
23533  |  PIK3R5  |  2.366  |  DISEASES
5328  |  PLAU  |  2.279  |  DISEASES
5464  |  PPA1  |  1.203  |  DISEASES
9055  |  PRC1  |  2.171  |  DISEASES
8842  |  PROM1  |  3.038  |  DISEASES
122183  |  PRR20A  |  2.286  |  DISEASES
729240  |  PRR20C  |  2.684  |  DISEASES
729250  |  PRR20E  |  2.684  |  DISEASES
5698  |  PSMB9  |  1.135  |  DISEASES
5728  |  PTEN  |  2.906  |  DISEASES
5743  |  PTGS2  |  2.544  |  DISEASES
5747  |  PTK2  |  1.135  |  DISEASES
53635  |  PTOV1  |  1.224  |  DISEASES
5789  |  PTPRD  |  1.647  |  DISEASES
80223  |  RAB11FIP1  |  1.825  |  DISEASES
5915  |  RARB  |  1.478  |  DISEASES
80196  |  RNF34  |  1.068  |  DISEASES
6120  |  RPE  |  1.638  |  DISEASES
6146  |  RPL22  |  1.252  |  DISEASES
6160  |  RPL31  |  2.118  |  DISEASES
864  |  RUNX3  |  1.984  |  DISEASES
6273  |  S100A2  |  2.168  |  DISEASES
6274  |  S100A3  |  1.646  |  DISEASES
6275  |  S100A4  |  1.574  |  DISEASES
6278  |  S100A7  |  1.241  |  DISEASES
6304  |  SATB1  |  1.536  |  DISEASES
29843  |  SENP1  |  1.763  |  DISEASES
26168  |  SENP3  |  1.772  |  DISEASES
5268  |  SERPINB5  |  2.946  |  DISEASES
6456  |  SH3GL2  |  2.495  |  DISEASES
6513  |  SLC2A1  |  3.063  |  DISEASES
23049  |  SMG1  |  1.441  |  DISEASES
23583  |  SMUG1  |  1.932  |  DISEASES
8651  |  SOCS1  |  1.076  |  DISEASES
6657  |  SOX2  |  2.115  |  DISEASES
347689  |  SOX2-OT  |  1.651  |  DISEASES
11262  |  SP140  |  1.41  |  DISEASES
6696  |  SPP1  |  1.551  |  DISEASES
6736  |  SRY  |  1.147  |  DISEASES
3925  |  STMN1  |  1.392  |  DISEASES
4070  |  TACSTD2  |  1.37  |  DISEASES
6925  |  TCF4  |  1.024  |  DISEASES
84260  |  TCHP  |  1.287  |  DISEASES
10178  |  TENM1  |  1.093  |  DISEASES
7053  |  TGM3  |  1.466  |  DISEASES
84000  |  TMPRSS13  |  1.257  |  DISEASES
8771  |  TNFRSF6B  |  1.986  |  DISEASES
8741  |  TNFSF13  |  1.263  |  DISEASES
7158  |  TP53BP1  |  1.057  |  DISEASES
7187  |  TRAF3  |  1.243  |  DISEASES
7323  |  UBE2D3  |  1.605  |  DISEASES
79465  |  ULBP3  |  1.383  |  DISEASES
7422  |  VEGFA  |  2.904  |  DISEASES
55135  |  WRAP53  |  1.483  |  DISEASES
331  |  XIAP  |  1.096  |  DISEASES
10771  |  ZMYND11  |  1.622  |  DISEASES
80139  |  ZNF703  |  1.557  |  DISEASES
7791  |  ZYX  |  1.009  |  DISEASES
Locus(Waiting for update.)
Disease ID 1729
Disease laryngeal carcinoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:9)
HP:0002860  |  Squamous cell carcinoma  |  21
HP:0002664  |  Neoplasia  |  11
HP:0030731  |  Carcinoma  |  3
HP:0100243  |  Leiomyosarcoma  |  1
HP:0001945  |  Fever  |  1
HP:0011459  |  Esophageal carcinoma  |  1
HP:0002835  |  Aspiration  |  1
HP:0000718  |  Aggressive behaviour  |  1
HP:0002840  |  Lymphadenitis  |  1
Disease ID 1729
Disease laryngeal carcinoma
Manually Symptom
UMLS  | Name(Total Manually Symptoms:19)
C2364133  |  infection
C2248595  |  dedifferentiation
C2239136  |  laryngocele
C1862463  |  aryl hydrocarbon hydroxylase inducibility
C1519670  |  tumor angiogenesis
C1306459  |  primary malignant neoplasm
C1135207  |  ataxia
C0694889  |  retinoblastoma
C0686619  |  lymph node metastases
C0684830  |  axillary metastasis
C0684249  |  lung cancer
C0153687  |  skin metastasis
C0042928  |  vocal cord paralysis
C0036467  |  tuberculous cervical lymphadenitis
C0024232  |  lymphatic metastasis
C0023524  |  progressive multifocal leucoencephalopathy
C0017168  |  gastroesophageal reflux disease
C0014118  |  endocarditis
C0001883  |  airway obstruction
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:4)
C0036467  |  tuberculous cervical lymphadenitis  |  1
C0009450  |  infection  |  1
C0265761  |  laryngocele  |  1
C0001883  |  airway obstruction  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:13)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs11615245632772067ERCC1umls:C0595989BeFreeIn summary, we suggest that genetic variations in ERCC1 rs11615 and ERCC5 rs17655 are associated with laryngeal cancer risk in a Chinese population, especially in ever smokers and drinkers.0.0008143262014ERCC11945420395AG
rs11615245829752073ERCC5umls:C0595989BeFreeIn conclusion, our study suggests that ERCC1 rs11615 and ERCC5 rs17655 polymorphisms are associated with increased risk of laryngeal cancer, and that they confer more risk among smokers and drinkers.0.0008143262014ERCC11945420395AG
rs11615245632772073ERCC5umls:C0595989BeFreeIn summary, we suggest that genetic variations in ERCC1 rs11615 and ERCC5 rs17655 are associated with laryngeal cancer risk in a Chinese population, especially in ever smokers and drinkers.0.0008143262014ERCC11945420395AG
rs122998421378355125ADH1Bumls:C0595989BeFreeAlcohol-dehydrogenase (ADH1B) Arg48His polymorphism in Basque Country patients with oral and laryngeal cancer: preliminary study.0.0005428842011ADH1B499318162TC
rs14286366575092797124TNFumls:C0595989BeFreeThe TNFR55-selective mutants (R32W, E146K and R32W-S86T) which bind poorly to TNFR75 displayed similar potency to wild-type TNF in causing cytotoxicity of a human laryngeal carcinoma-derived cell line (HEp-2) and cytostasis in a human leukaemic cell line (U937).0.0013572091994CUX17102111708GA
rs14286366575092791523CUX1umls:C0595989BeFreeThe TNFR55-selective mutants (R32W, E146K and R32W-S86T) which bind poorly to TNFR75 displayed similar potency to wild-type TNF in causing cytotoxicity of a human laryngeal carcinoma-derived cell line (HEp-2) and cytostasis in a human leukaemic cell line (U937).0.0002714421994CUX17102111708GA
rs14286366575092797132TNFRSF1Aumls:C0595989BeFreeThe TNFR55-selective mutants (R32W, E146K and R32W-S86T) which bind poorly to TNFR75 displayed similar potency to wild-type TNF in causing cytotoxicity of a human laryngeal carcinoma-derived cell line (HEp-2) and cytostasis in a human leukaemic cell line (U937).0.0002714421994CUX17102111708GA
rs17655245632772067ERCC1umls:C0595989BeFreeIn summary, we suggest that genetic variations in ERCC1 rs11615 and ERCC5 rs17655 are associated with laryngeal cancer risk in a Chinese population, especially in ever smokers and drinkers.0.0008143262014ERCC5;BIVM-ERCC513102875652GC
rs17655245632772073ERCC5umls:C0595989BeFreeIn summary, we suggest that genetic variations in ERCC1 rs11615 and ERCC5 rs17655 are associated with laryngeal cancer risk in a Chinese population, especially in ever smokers and drinkers.0.0008143262014ERCC5;BIVM-ERCC513102875652GC
rs17655245829752073ERCC5umls:C0595989BeFreeIn conclusion, our study suggests that ERCC1 rs11615 and ERCC5 rs17655 polymorphisms are associated with increased risk of laryngeal cancer, and that they confer more risk among smokers and drinkers.0.0008143262014ERCC5;BIVM-ERCC513102875652GC
rs25487241943937515XRCC1umls:C0595989BeFreeAssociation of XRCC1 genetic polymorphism (Arg399Gln) with laryngeal cancer: a meta-analysis based on 4,031 subjects.0.0005428842013XRCC11943551574TC
rs386493716241943937515XRCC1umls:C0595989BeFreeAssociation of XRCC1 genetic polymorphism (Arg399Gln) with laryngeal cancer: a meta-analysis based on 4,031 subjects.0.0005428842013NANANANANA
rs61754966240793634683NBNumls:C0595989BeFreeWe have previously shown that the p.I171V NBN gene mutation may contribute to the development of laryngeal cancer.0.0005428842013NBN889978293TC
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Disease ID 1729
Disease laryngeal carcinoma
Case(Waiting for update.)