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Pediatric Disease Annotations & Medicines



   generalized anxiety disorder
  

Disease ID 807
Disease generalized anxiety disorder
Definition
A condition marked by excessive worry and feelings of fear, dread, and uneasiness that last six months or longer. Other symptoms of GAD include being restless, being tired or irritable, muscle tension, not being able to concentrate or sleep well, shortness of breath, fast heartbeat, sweating, and dizziness.
Synonym
anxiety disorder generalize
anxiety disorder generalized
anxiety disorders generalized
gad
gad - generalised anxiety disorder
gad - generalized anxiety disorder
gads
generalised anxiety disorder
generalised anxiety disorder (disorder)
generalised anxiety disorder [ambiguous]
generalized anxiety dis
generalized anxiety disorder (disorder)
generalized anxiety disorders
OMIM
DOID
ICD10
UMLS
C0270549
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:28)
C0003467  |  anxiety  |  14
C0001818  |  agoraphobia  |  13
C0011570  |  depression  |  9
C0003469  |  anxiety disorder  |  5
C0003469  |  anxiety disorders  |  4
C0030319  |  panic disorder  |  3
C0041696  |  major depressive disorder  |  3
C0041696  |  major depression  |  2
C0006325  |  bruxism  |  2
C0031572  |  social phobia  |  2
C0012236  |  22q11.2 deletion syndrome  |  1
C0795690  |  omphalocele  |  1
C0037317  |  sleep disturbance  |  1
C0018799  |  heart disease  |  1
C0236801  |  specific phobia  |  1
C0019196  |  hepatitis c  |  1
C0032460  |  polycystic ovary syndrome  |  1
C0032460  |  polycystic ovary  |  1
C0236792  |  asperger's disorder  |  1
C0040128  |  thyroid disorders  |  1
C0851578  |  sleep disorders  |  1
C0013395  |  dyspepsia  |  1
C0013415  |  dysthymic disorder  |  1
C0019158  |  hepatitis  |  1
C0038436  |  posttraumatic stress disorder  |  1
C0948265  |  metabolic syndrome  |  1
C0037317  |  sleep disturbances  |  1
C0010068  |  coronary heart disease  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:2)
GRAP2  |  9402  |  OMIM
GAD1  |  2571  |  OMIM
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:151)
4710  |  NDUFB4  |  DISEASES
27248  |  ERLEC1  |  DISEASES
6530  |  SLC6A2  |  DISEASES
1158  |  CKM  |  DISEASES
41  |  ASIC1  |  DISEASES
55907  |  CMAS  |  DISEASES
23438  |  HARS2  |  DISEASES
2908  |  NR3C1  |  DISEASES
11334  |  TUSC2  |  DISEASES
5997  |  RGS2  |  DISEASES
134637  |  ADAT2  |  DISEASES
140735  |  DYNLL2  |  DISEASES
7291  |  TWIST1  |  DISEASES
5552  |  SRGN  |  DISEASES
5184  |  PEPD  |  DISEASES
5880  |  RAC2  |  DISEASES
7166  |  TPH1  |  DISEASES
8220  |  DGCR14  |  DISEASES
7136  |  TNNI2  |  DISEASES
9113  |  LATS1  |  DISEASES
8572  |  PDLIM4  |  DISEASES
55145  |  THAP1  |  DISEASES
51540  |  SCLY  |  DISEASES
1401  |  CRP  |  DISEASES
3357  |  HTR2B  |  DISEASES
2572  |  GAD2  |  DISEASES
6519  |  SLC3A1  |  DISEASES
9360  |  PPIG  |  DISEASES
3093  |  UBE2K  |  DISEASES
6532  |  SLC6A4  |  DISEASES
4969  |  OGN  |  DISEASES
2033  |  EP300  |  DISEASES
8452  |  CUL3  |  DISEASES
51665  |  ASB1  |  DISEASES
5443  |  POMC  |  DISEASES
64083  |  GOLPH3  |  DISEASES
55749  |  CCAR1  |  DISEASES
56938  |  ARNTL2  |  DISEASES
93650  |  ACPT  |  DISEASES
3756  |  KCNH1  |  DISEASES
3358  |  HTR2C  |  DISEASES
1392  |  CRH  |  DISEASES
5047  |  PAEP  |  DISEASES
150  |  ADRA2A  |  DISEASES
51594  |  NBAS  |  DISEASES
55079  |  FEZF2  |  DISEASES
6529  |  SLC6A1  |  DISEASES
4681  |  NBL1  |  DISEASES
2560  |  GABRB1  |  DISEASES
50852  |  TRAT1  |  DISEASES
6632  |  SNRPD1  |  DISEASES
6786  |  STIM1  |  DISEASES
4054  |  LTBP3  |  DISEASES
116844  |  LRG1  |  DISEASES
140738  |  TMEM37  |  DISEASES
51181  |  DCXR  |  DISEASES
6869  |  TACR1  |  DISEASES
1816  |  DRD5  |  DISEASES
255239  |  ANKK1  |  DISEASES
1501  |  CTNND2  |  DISEASES
134  |  ADORA1  |  DISEASES
51172  |  NAGPA  |  DISEASES
10713  |  USP39  |  DISEASES
3352  |  HTR1D  |  DISEASES
3350  |  HTR1A  |  DISEASES
147912  |  SIX5  |  DISEASES
4026  |  LPP  |  DISEASES
10938  |  EHD1  |  DISEASES
6863  |  TAC1  |  DISEASES
7156  |  TOP3A  |  DISEASES
23017  |  FAIM2  |  DISEASES
5021  |  OXTR  |  DISEASES
1812  |  DRD1  |  DISEASES
5074  |  PAWR  |  DISEASES
706  |  TSPO  |  DISEASES
277  |  AMY1B  |  DISEASES
5136  |  PDE1A  |  DISEASES
170392  |  OIT3  |  DISEASES
887  |  CCKBR  |  DISEASES
3988  |  LIPA  |  DISEASES
64359  |  NXN  |  DISEASES
3363  |  HTR7  |  DISEASES
9402  |  GRAP2  |  DISEASES
6540  |  SLC6A13  |  DISEASES
4128  |  MAOA  |  DISEASES
1395  |  CRHR2  |  DISEASES
1544  |  CYP1A2  |  DISEASES
1508  |  CTSB  |  DISEASES
132884  |  EVC2  |  DISEASES
10166  |  SLC25A15  |  DISEASES
5348  |  FXYD1  |  DISEASES
23481  |  PES1  |  DISEASES
3359  |  HTR3A  |  DISEASES
5979  |  RET  |  DISEASES
51114  |  ZDHHC9  |  DISEASES
2571  |  GAD1  |  DISEASES
8936  |  WASF1  |  DISEASES
6539  |  SLC6A12  |  DISEASES
387129  |  NPSR1  |  DISEASES
1066  |  CES1  |  DISEASES
11169  |  WDHD1  |  DISEASES
1565  |  CYP2D6  |  DISEASES
5167  |  ENPP1  |  DISEASES
1312  |  COMT  |  DISEASES
4860  |  PNP  |  DISEASES
1813  |  DRD2  |  DISEASES
7058  |  THBS2  |  DISEASES
2058  |  EPRS  |  DISEASES
5362  |  PLXNA2  |  DISEASES
2494  |  NR5A2  |  DISEASES
4014  |  LOR  |  DISEASES
3713  |  IVL  |  DISEASES
3351  |  HTR1B  |  DISEASES
278  |  AMY1C  |  DISEASES
276  |  AMY1A  |  DISEASES
115004  |  MB21D1  |  DISEASES
81030  |  ZBP1  |  DISEASES
11128  |  POLR3A  |  DISEASES
79717  |  PPCS  |  DISEASES
23569  |  PADI4  |  DISEASES
1325  |  CORT  |  DISEASES
4129  |  MAOB  |  DISEASES
3356  |  HTR2A  |  DISEASES
2625  |  GATA3  |  DISEASES
146  |  ADRA1D  |  DISEASES
148  |  ADRA1A  |  DISEASES
1814  |  DRD3  |  DISEASES
9901  |  SRGAP3  |  DISEASES
3426  |  CFI  |  DISEASES
5660  |  PSAP  |  DISEASES
2912  |  GRM2  |  DISEASES
1394  |  CRHR1  |  DISEASES
210  |  ALAD  |  DISEASES
9048  |  ARTN  |  DISEASES
348180  |  CTU2  |  DISEASES
65250  |  C5orf42  |  DISEASES
23210  |  JMJD6  |  DISEASES
10163  |  WASF2  |  DISEASES
8910  |  SGCE  |  DISEASES
6635  |  SNRPE  |  DISEASES
9278  |  ZBTB22  |  DISEASES
83871  |  RAB34  |  DISEASES
389549  |  FEZF1  |  DISEASES
627  |  BDNF  |  DISEASES
3035  |  HARS  |  DISEASES
54970  |  TTC12  |  DISEASES
4925  |  NUCB2  |  DISEASES
5715  |  PSMD9  |  DISEASES
169355  |  IDO2  |  DISEASES
91056  |  AP5B1  |  DISEASES
4782  |  NFIC  |  DISEASES
Locus(Waiting for update.)
Disease ID 807
Disease generalized anxiety disorder
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:17)
HP:0000739  |  Anxiety  |  14
HP:0000756  |  Fear of open spaces  |  13
HP:0000716  |  Depression  |  9
HP:0003763  |  Bruxism  |  2
HP:0011675  |  Arrhythmias  |  1
HP:0001539  |  Omphalocele  |  1
HP:0001397  |  Hepatic steatosis  |  1
HP:0000360  |  Ringing in the ears  |  1
HP:0002315  |  Headaches  |  1
HP:0012115  |  Liver inflammation  |  1
HP:0000147  |  Sclerocystic ovaries  |  1
HP:0001511  |  Prenatal onset growth retardation  |  1
HP:0100710  |  Impulsivity  |  1
HP:0000708  |  Behavioral problems  |  1
HP:0002500  |  Leukoaraiosis  |  1
HP:0002360  |  Sleep disturbance  |  1
HP:0100543  |  Cognitive deficits  |  1
Disease ID 807
Disease generalized anxiety disorder
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
C0011570  |  depression  |  9
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:12)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1245471220122683596BCL2umls:C0270549BeFreeBCL2 rs12454712 (p = .0029) and DRD2 rs4245146 (p = .0010) showed evidence for association to generalized anxiety disorder, whereas rs2463107 (p = .0064) in PAWR and rs4245146 (p = .0029) in DRD2 showed evidence for association to the pooled group of all anxiety disorders.0.0002714422010BCL21863178651TC
rs12454712201226835074PAWRumls:C0270549BeFreeBCL2 rs12454712 (p = .0029) and DRD2 rs4245146 (p = .0010) showed evidence for association to generalized anxiety disorder, whereas rs2463107 (p = .0064) in PAWR and rs4245146 (p = .0029) in DRD2 showed evidence for association to the pooled group of all anxiety disorders.0.0002714422010BCL21863178651TC
rs12454712201226831813DRD2umls:C0270549BeFreeBCL2 rs12454712 (p = .0029) and DRD2 rs4245146 (p = .0010) showed evidence for association to generalized anxiety disorder, whereas rs2463107 (p = .0064) in PAWR and rs4245146 (p = .0029) in DRD2 showed evidence for association to the pooled group of all anxiety disorders.0.0005428842010BCL21863178651TC
rs2463107201226831813DRD2umls:C0270549BeFreeBCL2 rs12454712 (p = .0029) and DRD2 rs4245146 (p = .0010) showed evidence for association to generalized anxiety disorder, whereas rs2463107 (p = .0064) in PAWR and rs4245146 (p = .0029) in DRD2 showed evidence for association to the pooled group of all anxiety disorders.0.0005428842010NA1279699537AC
rs246310720122683596BCL2umls:C0270549BeFreeBCL2 rs12454712 (p = .0029) and DRD2 rs4245146 (p = .0010) showed evidence for association to generalized anxiety disorder, whereas rs2463107 (p = .0064) in PAWR and rs4245146 (p = .0029) in DRD2 showed evidence for association to the pooled group of all anxiety disorders.0.0002714422010NA1279699537AC
rs2463107201226835074PAWRumls:C0270549BeFreeBCL2 rs12454712 (p = .0029) and DRD2 rs4245146 (p = .0010) showed evidence for association to generalized anxiety disorder, whereas rs2463107 (p = .0064) in PAWR and rs4245146 (p = .0029) in DRD2 showed evidence for association to the pooled group of all anxiety disorders.0.0002714422010NA1279699537AC
rs386602276114446843356HTR2Aumls:C0270549BeFreeThe authors tested for association of the 5-HT2A receptor polymorphism (T102C) and the intron 7 tryptophan hydroxylase (TPH) polymorphism (A218C) among 176 alcohol dependent patients, 35 patients with panic disorder, 50 patients with generalized anxiety disorder, 55 patients with narcolepsy and 87 healthy controls.0.0008143262001NANANANANA
rs424514620122683596BCL2umls:C0270549BeFreeBCL2 rs12454712 (p = .0029) and DRD2 rs4245146 (p = .0010) showed evidence for association to generalized anxiety disorder, whereas rs2463107 (p = .0064) in PAWR and rs4245146 (p = .0029) in DRD2 showed evidence for association to the pooled group of all anxiety disorders.0.0002714422010DRD211113447251TC
rs4245146201226835074PAWRumls:C0270549BeFreeBCL2 rs12454712 (p = .0029) and DRD2 rs4245146 (p = .0010) showed evidence for association to generalized anxiety disorder, whereas rs2463107 (p = .0064) in PAWR and rs4245146 (p = .0029) in DRD2 showed evidence for association to the pooled group of all anxiety disorders.0.0002714422010DRD211113447251TC
rs4245146201226831813DRD2umls:C0270549BeFreeBCL2 rs12454712 (p = .0029) and DRD2 rs4245146 (p = .0010) showed evidence for association to generalized anxiety disorder, whereas rs2463107 (p = .0064) in PAWR and rs4245146 (p = .0029) in DRD2 showed evidence for association to the pooled group of all anxiety disorders.0.0005428842010DRD211113447251TC
rs4792888222493551394CRHR1umls:C0270549BeFreeOnly rs4792888 in CRHR1 showed modest evidence of association with duloxetine response in MDD (P=0.029 in GAD, P=0.054 in MDD).0.0005428842013CRHR1;MGC57346-CRHR11745800588AG
rs6313114446843356HTR2Aumls:C0270549BeFreeThe authors tested for association of the 5-HT2A receptor polymorphism (T102C) and the intron 7 tryptophan hydroxylase (TPH) polymorphism (A218C) among 176 alcohol dependent patients, 35 patients with panic disorder, 50 patients with generalized anxiety disorder, 55 patients with narcolepsy and 87 healthy controls.0.0008143262001HTR2A1346895805GA
GWASdb Annotation(Total Genotypes:10)
Chr Pos SNP_Id RefGene EnsemblGene ENCODE_Factor ENCODE_TFBS Chromosome_interaction GTEx_eQTL SNP_TFBS_affinity_GWAS3D SNP_miRNA_target_affinity_PolymiRTS SNP_splicing_effect_Skippy SNP_splicing_effect_MutPred_Splice SNP_ns_protein_effect_dbNSFP SNP_syn_effect_Silva SNP_phosphorylation_effect_PhosSNP PhastCons_score PhyloP_score GERP++_RS Segway_state Ancestral_allele ESP_AF ESP_AFR ESP_AFR ESP_EUR TG_ASN TG_AMR TG_AFR TG_EUR Type Consequence bStatistic EncH3K27Ac EncH3K4Me1 EncH3K4Me3 EncNucleo OMIM Clinvar
2171688593rs10191129NM_000817,GAD1NM_013445,GAD1ENST00000358196,ENSG00000128683ENST00000375273,ENSG00000128683ENST00000493875,ENSG00000128683ENST00000414527,ENSG00000128683ENST00000375272,ENSG00000128683ENST00000344257,ENSG00000128683ENST00000429023,ENSG00000128683ENST00000493270,ENSG00000128683MCV-2NAchr2,171680001,171690000,chr9,44590001,44600000,18,Hi-CNACha4-primary,3.4605Cutl1_3494,1.4168Gln3-primary,1.544Gzf3-primary,1.9512Hoxc13_3127,1.3052NANANANANANA0.0380.3801.43GM0CNANANANANA
2171695070rs3791853NM_000817,GAD1NM_013445,GAD1ENST00000358196,ENSG00000128683ENST00000375273,ENSG00000128683ENST00000493875,ENSG00000128683ENST00000414527,ENSG00000128683ENST00000375272,ENSG00000128683ENST00000344257,ENSG00000128683ENST00000429023,ENSG00000128683NANAchr2,171690001,171700000,chr12,88780001,88790000,4,Hi-Cchr2,171690001,171700000,chr2,172330001,172340000,5,Hi-Cchr2,171690001,171700000,chr14,39570001,39580000,6,Hi-CNALys14-primary,1.4423Pho2-DBD-primary,3.5931Smp1-primary,4.7276Yrm1-primary,2.1908Yrr1-FL-primary,1.4803NANANANANANA0.000-0.344-2.13R4GNANANANA
2240303934rs137963NM_004810,GRAP2ENST00000344138,ENSG00000100351MCV-4TFP.USF2NAchr22,40300001,40310000,chr22,40930001,40940000,7,Hi-Cchr22,40300001,40310000,chr10,37260001,37270000,8,Hi-Cchr22,40300001,40310000,chr2,61030001,61040000,8,Hi-CNALM90,1.4251LM90,1.5106LM120,2.0575LM128,1.3303Arnt,10.7157NANANANANANA0.000-1.984-4.81GM1CNANANANANANANANATranscriptINTRONIC
2240320361rs137977NM_004810,GRAP2ENST00000344138,ENSG00000100351NANANANACutl1_3494,3.842Cutl1_3494,7.3201Hoxa5_3415,5.0077Hoxc8_3429,10.1588Rsc3-primary,1.9231NANANANANANA0.000-0.0140.112TF2ANANANA0.6000.7400.4700.8400.420TranscriptINTRONIC6671.085.64
2240336845rs137989NM_004810,GRAP2ENST00000344138,ENSG00000100351ENST00000420971,ENSG00000100351ENST00000478445,ENSG00000100351ENST00000461082,ENSG00000100351MCV-4TFP.RAD21TFP.SMC3TFP.CTCFNANANAPax-5,3.683Cart-1,1.6686HTF,9.003RFX,5.1188FOXP3,3.726NANANANANANA0.0010.9102.93C1TNANANANANANANA
2240340775rs137991NM_004810,GRAP2ENST00000344138,ENSG00000100351ENST00000420971,ENSG00000100351ENST00000478445,ENSG00000100351ENST00000461082,ENSG00000100351NANAchr22,40340001,40350000,chr9,113170001,113180000,6,Hi-Cchr22,40340001,40350000,chr10,81960001,81970000,7,Hi-Cchr22,40340001,40350000,chr12,69000001,69010000,6,Hi-Cchr22,40340001,40350000,chr15,74640001,74650000,9,Hi-CNAGal4-primary,1.3497Gal4-primary,1.3403Lhx6_2272,2.3444Rph1-primary,1.7391LM134,2.2951NANANANANANA0.0010.1990.926E/GMTNANANANANANANA
2240348520rs2267420NM_004810,GRAP2ENST00000344138,ENSG00000100351ENST00000420971,ENSG00000100351ENST00000478445,ENSG00000100351ENST00000407075,ENSG00000100351MCV-4NAchr22,40340001,40350000,chr9,113170001,113180000,6,Hi-Cchr22,40340001,40350000,chr10,81960001,81970000,7,Hi-Cchr22,40340001,40350000,chr12,69000001,69010000,6,Hi-Cchr22,40340001,40350000,chr15,74640001,74650000,9,Hi-CNACha4-primary,1.5884Mig2-primary,1.5883Mig3-primary,1.3813Pbf1-primary,1.6666Pbf2-primary,2.4298NANANANANANA0.000-0.710-4.36GM1ANANANA0.1100.1200.1100.020
2240357667rs9611234NM_004810,GRAP2ENST00000344138,ENSG00000100351ENST00000478445,ENSG00000100351ENST00000407075,ENSG00000100351ENST00000424496,ENSG00000225528TFP.CEBPBTFP.STAT3TFP.TCF12TFP.FOSL1TFP.EP300TFP.JUNDTFP.MAXCHMMTFP.HDAC2TFP.JUNTFP.E2F6TFP.FOSTFP.JUNBTFP.MYCTFP.PAX5TFP.MAFKTFP.IRF4TFP.BCL11ATFP.RXRATFP.GATA2TFP.CCNT2TFP.BATFTFP.TAL1TFP.POU2F2MCV-85NAchr22,40350001,40360000,chr2,96710001,96720000,246,Hi-Cchr22,40350001,40360000,chr4,190700001,190710000,5,Hi-CNALM9,3.4226
2240362946rs138006NM_004810,GRAP2ENST00000344138,ENSG00000100351ENST00000478445,ENSG00000100351ENST00000407075,ENSG00000100351ENST00000481263,ENSG00000100351TFP.JUNDCHMMTFP.CEBPBTFP.EP300TFP.TBPTFP.STAT3TFP.GATA1MCV-2NAchr22,40360001,40370000,chr19,14300001,14310000,30,Hi-Cchr22,40360001,40370000,chr22,39010001,39020000,5,Hi-Cchr22,40360001,40370000,chr22,42970001,42980000,12,Hi-CNAMEF-2,1.3035PR,1.2838PR,1.2639SRF,16.2319NANANANANANA0.0000.2680.814E/GMGNANA
2240363778rs2284078NM_004810,GRAP2ENST00000344138,ENSG00000100351ENST00000407075,ENSG00000100351ENST00000481263,ENSG00000100351CHMMTFP.CEBPBTFP.TBPTFP.GATA1TFP.TFAP2CTFP.TFAP2ATFP.EP300TFP.GATA2TFP.CCNT2TFP.TAL1NAchr22,40360001,40370000,chr19,14300001,14310000,30,Hi-Cchr22,40360001,40370000,chr22,39010001,39020000,5,Hi-Cchr22,40360001,40370000,chr22,42970001,42980000,12,Hi-CNANkx2-9_3082,1.8884Obox1_3970,1.3041Obox6_3440,2.3031Rsc30-primary,1.3003Rsc30-primary,2.1369NANANANANANA0.000-0.591-2.68GM0A
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.)
Chemical(Total Drugs:0)
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FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)