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Pediatric Disease Annotations & Medicines



   varicocele
  

Disease ID 718
Disease varicocele
Definition
A condition characterized by the dilated tortuous veins of the SPERMATIC CORD with a marked left-sided predominance. Adverse effect on male fertility occurs when varicocele leads to an increased scrotal (and testicular) temperature and reduced testicular volume.
Synonym
scrotal varices
scrotal varices (disorder)
scrotal varices - varicocele
scrotal varicose veins
scrotum varicose vein
scrotum varicose veins
vaginal varicocele
varicocele (disorder)
varicocele [ambiguous]
varicocele [disease/finding]
varicoceles
varicocoele
varicole
varicoles
varicose veins scrotum
DOID
ICD10
UMLS
C0042341
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:23)
C0021359  |  infertile  |  72
C0021359  |  infertility  |  31
C0021364  |  male infertility  |  15
C0042345  |  varicose veins  |  5
C0004509  |  azoospermia  |  5
C0042345  |  varicose vein  |  5
C0020619  |  hypogonadism  |  2
C0405581  |  testicular dysfunction  |  2
C0028960  |  oligospermia  |  2
C0152078  |  pelvic congestion syndrome  |  1
C0004943  |  behcet disease  |  1
C0011849  |  diabetes mellitus  |  1
C0028960  |  oligozoospermia  |  1
C0242350  |  erectile dysfunction  |  1
C0038012  |  spondylitis  |  1
C0009806  |  constipation  |  1
C0011649  |  dermoid cyst  |  1
C0011649  |  dermoid cysts  |  1
C0038013  |  ankylosing spondylitis  |  1
C0011847  |  diabetes  |  1
C0156312  |  testicular atrophy  |  1
C0019294  |  inguinal hernia  |  1
C0152078  |  pelvic congestion  |  1
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:2)
2944  |  GSTM1  |  infer
2952  |  GSTT1  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:161)
10942  |  PRSS21  |  DISEASES
5010  |  CLDN11  |  DISEASES
6793  |  STK10  |  DISEASES
54763  |  ROPN1  |  DISEASES
7414  |  VCL  |  DISEASES
513  |  ATP5D  |  DISEASES
9567  |  GTPBP1  |  DISEASES
49  |  ACR  |  DISEASES
140679  |  SLC32A1  |  DISEASES
412  |  STS  |  DISEASES
366  |  AQP9  |  DISEASES
51285  |  RASL12  |  DISEASES
2137  |  EXTL3  |  DISEASES
3972  |  LHB  |  DISEASES
1158  |  CKM  |  DISEASES
268  |  AMH  |  DISEASES
973  |  CD79A  |  DISEASES
1819  |  DRG2  |  DISEASES
116449  |  CLNK  |  DISEASES
4254  |  KITLG  |  DISEASES
7141  |  TNP1  |  DISEASES
5620  |  PRM2  |  DISEASES
7291  |  TWIST1  |  DISEASES
5184  |  PEPD  |  DISEASES
1446  |  CSN1S1  |  DISEASES
1773  |  DNASE1  |  DISEASES
3306  |  HSPA2  |  DISEASES
3315  |  HSPB1  |  DISEASES
2952  |  GSTT1  |  DISEASES
5908  |  RAP1B  |  DISEASES
9210  |  BMP15  |  DISEASES
2488  |  FSHB  |  DISEASES
269  |  AMHR2  |  DISEASES
3569  |  IL6  |  DISEASES
10068  |  IL18BP  |  DISEASES
5687  |  PSMA6  |  DISEASES
384  |  ARG2  |  DISEASES
4016  |  LOXL1  |  DISEASES
5052  |  PRDX1  |  DISEASES
27178  |  IL37  |  DISEASES
51192  |  CKLF  |  DISEASES
9595  |  CYTIP  |  DISEASES
8807  |  IL18RAP  |  DISEASES
5443  |  POMC  |  DISEASES
89869  |  PLCZ1  |  DISEASES
22822  |  PHLDA1  |  DISEASES
122481  |  AK7  |  DISEASES
146225  |  CMTM2  |  DISEASES
409  |  ARRB2  |  DISEASES
7157  |  TP53  |  DISEASES
93650  |  ACPT  |  DISEASES
52  |  ACP1  |  DISEASES
5972  |  REN  |  DISEASES
2796  |  GNRH1  |  DISEASES
6770  |  STAR  |  DISEASES
4715  |  NDUFB9  |  DISEASES
133  |  ADM  |  DISEASES
3948  |  LDHC  |  DISEASES
7082  |  TJP1  |  DISEASES
27306  |  HPGDS  |  DISEASES
60675  |  PROK2  |  DISEASES
3490  |  IGFBP7  |  DISEASES
213  |  ALB  |  DISEASES
7047  |  TGM4  |  DISEASES
308  |  ANXA5  |  DISEASES
2661  |  GDF9  |  DISEASES
4846  |  NOS3  |  DISEASES
6866  |  TAC3  |  DISEASES
915  |  CD3D  |  DISEASES
29123  |  ANKRD11  |  DISEASES
5617  |  PRL  |  DISEASES
23440  |  OTP  |  DISEASES
8988  |  HSPB3  |  DISEASES
86614  |  HSFY1  |  DISEASES
159119  |  HSFY2  |  DISEASES
948  |  CD36  |  DISEASES
6954  |  TCP11  |  DISEASES
8793  |  TNFRSF10D  |  DISEASES
5619  |  PRM1  |  DISEASES
836  |  CASP3  |  DISEASES
2944  |  GSTM1  |  DISEASES
8557  |  TCAP  |  DISEASES
3952  |  LEP  |  DISEASES
354  |  KLK3  |  DISEASES
1191  |  CLU  |  DISEASES
283417  |  DPY19L2  |  DISEASES
3640  |  INSL3  |  DISEASES
1153  |  CIRBP  |  DISEASES
2274  |  FHL2  |  DISEASES
7525  |  YES1  |  DISEASES
9622  |  KLK4  |  DISEASES
10693  |  CCT6B  |  DISEASES
4843  |  NOS2  |  DISEASES
9083  |  BPY2  |  DISEASES
7639  |  ZNF85  |  DISEASES
842  |  CASP9  |  DISEASES
3953  |  LEPR  |  DISEASES
9112  |  MTA1  |  DISEASES
881  |  CCIN  |  DISEASES
3320  |  HSP90AA1  |  DISEASES
3091  |  HIF1A  |  DISEASES
7180  |  CRISP2  |  DISEASES
5764  |  PTN  |  DISEASES
64518  |  TEKT3  |  DISEASES
889  |  KRIT1  |  DISEASES
9260  |  PDLIM7  |  DISEASES
8881  |  CDC16  |  DISEASES
8794  |  TNFRSF10C  |  DISEASES
841  |  CASP8  |  DISEASES
79947  |  DHDDS  |  DISEASES
4508  |  MT-ATP6  |  DISEASES
9760  |  TOX  |  DISEASES
4513  |  MT-CO2  |  DISEASES
4537  |  MT-ND3  |  DISEASES
4509  |  MT-ATP8  |  DISEASES
142  |  PARP1  |  DISEASES
356  |  FASLG  |  DISEASES
6283  |  S100A12  |  DISEASES
3283  |  HSD3B1  |  DISEASES
55361  |  PI4K2A  |  DISEASES
1791  |  DNTT  |  DISEASES
729238  |  SFTPA2  |  DISEASES
6407  |  SEMG2  |  DISEASES
6406  |  SEMG1  |  DISEASES
5225  |  PGC  |  DISEASES
246184  |  CDC26  |  DISEASES
3304  |  HSPA1B  |  DISEASES
7407  |  VARS  |  DISEASES
3055  |  HCK  |  DISEASES
29968  |  PSAT1  |  DISEASES
9563  |  H6PD  |  DISEASES
57126  |  CD177  |  DISEASES
3980  |  LIG3  |  DISEASES
5212  |  VIT  |  DISEASES
5251  |  PHEX  |  DISEASES
6462  |  SHBG  |  DISEASES
83605  |  CCM2  |  DISEASES
2813  |  GP2  |  DISEASES
442868  |  BPY2C  |  DISEASES
442867  |  BPY2B  |  DISEASES
6736  |  SRY  |  DISEASES
174  |  AFP  |  DISEASES
1617  |  DAZ1  |  DISEASES
7018  |  TF  |  DISEASES
23066  |  CAND2  |  DISEASES
4295  |  MLN  |  DISEASES
5601  |  MAPK9  |  DISEASES
2674  |  GFRA1  |  DISEASES
653509  |  SFTPA1  |  DISEASES
7124  |  TNF  |  DISEASES
57135  |  DAZ4  |  DISEASES
5706  |  PSMC6  |  DISEASES
9278  |  ZBTB22  |  DISEASES
6628  |  SNRPB  |  DISEASES
8260  |  NAA10  |  DISEASES
4700  |  NDUFA6  |  DISEASES
4671  |  NAIP  |  DISEASES
917  |  CD3G  |  DISEASES
3316  |  HSPB2  |  DISEASES
414768  |  HCG24  |  DISEASES
102723508  |  KANTR  |  DISEASES
Locus(Waiting for update.)
Disease ID 718
Disease varicocele
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:17)
HP:0000789  |  Infertility  |  31
HP:0003251  |  Male infertility  |  15
HP:0012531  |  Pain  |  8
HP:0002619  |  Varicose veins  |  5
HP:0000027  |  Azoospermia  |  5
HP:0011962  |  Obstructive azoospermia  |  3
HP:0000135  |  Hypogonadism  |  2
HP:0000798  |  Oligospermia  |  2
HP:0030155  |  Scrotal pain  |  2
HP:0002019  |  Dyschezia  |  1
HP:0000023  |  Inguinal hernia  |  1
HP:0000802  |  Erectile dysfunction  |  1
HP:0100790  |  Hernia  |  1
HP:0012450  |  Chronic constipation  |  1
HP:0200040  |  Epidermal inclusion cyst  |  1
HP:0000819  |  Diabetes mellitus  |  1
HP:0000029  |  Testicular degeneration  |  1
Disease ID 718
Disease varicocele
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:10)
C0021359  |  infertility  |  31
C0021364  |  male infertility  |  15
C0030193  |  pain  |  8
C0004509  |  azoospermia  |  5
C0236078  |  scrotal pain  |  2
C0405581  |  testicular dysfunction  |  2
C0156312  |  testicular atrophy  |  1
C0729353  |  subfertility  |  1
C2363955  |  venous reflux  |  1
C0039591  |  orchialgia  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:1)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs397507444244561054524MTHFRumls:C0042341BeFreeIs methylenetetrahydrofolate reductase (MTHFR) gene A1298C polymorphism related with varicocele risk?0.0002714422013MTHFR111794407TG
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.)
Chemical(Total Drugs:2)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0042341diethylstilbestrolD00405456-53-1varicoceleMESH:D014646marker/mechanism7463583
C0042341nitric oxideD00956910102-43-9varicoceleMESH:D014646marker/mechanism18572859
FDA approved drug and dosage information(Total Drugs:1)
DiseaseID Drug_name active_ingredients strength Dosage Form/Route Marketing Status TE code RLD RS
MESH:D014646inomaxnitric oxide100PPM Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasonsGAS;INHALATIONDiscontinuedNoneYesNo
FDA labeling changes(Total Drugs:1)
DiseaseID Pediatric_Labeling_Date Trade_Name Generic_Name_or_Proper_Name Indications Studied Label Changes Summary Product Labeling BPCA(B) PREA(P) BPCA(B) and PREA(P) Pediatric Rule (R) Sponsor Pediatric Exclusivity Granted Date NNPS
MESH:D01464612/21/2010inomaxnitric oxidePrevention of bronchopulmonary dysplasiaINOmax is not indicated for prevention of BPD in preterm neonates d 34 weeks gestational age.Efficacy for the prevention of BPD in preterm infants was not established in three ldouble-blind, placebo-controlled clinical trials in a total of 2,149 preterm infants Information on clinical trials, adverse reactionLabelingB---INO Therapeutics2/11/2010FALSE'