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Pediatric Disease Annotations & Medicines



   alcohol abuse
  

Disease ID 1817
Disease alcohol abuse
Definition
The use of alcoholic beverages to excess, either on individual occasions ("binge drinking") or as a regular practice.
Synonym
aa - alcohol abuse
abuse, alcohol
alcohol abuse (disorder)
alcohol abuse disorder
alcohol abuse, unspecified
alcohol abuse, unspecified drinking behavior
alcohol abuse-unspec
alcohol abuses
drinking problem
drinking problems
dysfunctional alcohol use
ethanol abuse
ethanol abuse (finding)
etoh abuse
problem drinking
DOID
UMLS
C0085762
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:79)
C0023890  |  cirrhosis  |  16
C0023895  |  liver disease  |  13
C0030305  |  pancreatitis  |  12
C0023890  |  liver cirrhosis  |  10
C0011570  |  depression  |  8
C0003467  |  anxiety  |  8
C0019158  |  hepatitis  |  5
C0011847  |  diabetes  |  5
C0020538  |  hypertension  |  5
C0042373  |  vascular disease  |  4
C0001339  |  acute pancreatitis  |  4
C0036341  |  schizophrenia  |  3
C0497327  |  dementia  |  3
C0005586  |  bipolar disorder  |  3
C0004936  |  mental disorders  |  2
C0149521  |  chronic pancreatitis  |  2
C0019163  |  hepatitis b  |  2
C0029456  |  osteoporosis  |  2
C0948265  |  metabolic syndrome  |  2
C0039841  |  thiamine deficiency  |  2
C0023895  |  hepatopathy  |  2
C0003469  |  anxiety disorder  |  2
C0033975  |  psychosis  |  2
C0023895  |  hepatic disorders  |  2
C0037317  |  sleep disturbance  |  2
C0019151  |  hepatic encephalopathy  |  2
C0028754  |  obesity  |  2
C0023895  |  hepatic disease  |  2
C0004623  |  bacterial infection  |  2
C0040188  |  tic disorders  |  2
C0016412  |  folate deficiency  |  1
C0270549  |  generalized anxiety disorder  |  1
C0349464  |  wernicke-korsakoff syndrome  |  1
C0085580  |  essential hypertension  |  1
C0162429  |  nutritional deficiencies  |  1
C0040034  |  thrombocytopenia  |  1
C0031090  |  periodontal disease  |  1
C0376670  |  alcoholic pancreatitis  |  1
C0022116  |  ischaemia  |  1
C0023364  |  leptospirosis  |  1
C0033975  |  psychotic disorder  |  1
C0001957  |  delirium tremens  |  1
C0040425  |  tonsillitis  |  1
C0004134  |  ataxia  |  1
C0011849  |  diabetes mellitus  |  1
C0878544  |  cardiomyopathy  |  1
C0031212  |  personality disorders  |  1
C0018799  |  heart disease  |  1
C0149654  |  conduct disorder  |  1
C0023895  |  liver disorders  |  1
C0022658  |  renal disease  |  1
C0002395  |  alzheimer's disease  |  1
C0023895  |  liver disorder  |  1
C0018801  |  heart failure  |  1
C0030662  |  pathological gambling  |  1
C0003469  |  anxiety disorders  |  1
C0017152  |  gastritis  |  1
C0007222  |  cardiovascular disease  |  1
C0019196  |  hepatitis c  |  1
C0349464  |  korsakoff syndrome  |  1
C0032285  |  pneumonia  |  1
C0042769  |  virus infection  |  1
C0021053  |  immune dysfunction  |  1
C0028756  |  severe obesity  |  1
C0021390  |  inflammatory bowel disease  |  1
C0023895  |  liver diseases  |  1
C0004626  |  bacterial pneumonia  |  1
C0041696  |  major depression  |  1
C0001973  |  alcoholism  |  1
C0008350  |  gall stone  |  1
C0851578  |  sleep disorders  |  1
C0162429  |  malnutrition  |  1
C0023801  |  madelung's disease  |  1
C0019204  |  hepatocellular carcinoma  |  1
C0014544  |  epilepsy  |  1
C0007193  |  dilated cardiomyopathy  |  1
C0037317  |  sleep disturbances  |  1
C0014544  |  epileptic fits  |  1
C0020676  |  hypothyroidism  |  1
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:42)
125  |  ADH1B  |  infer
126  |  ADH1C  |  infer
127  |  ADH4  |  infer
216  |  ALDH1A1  |  infer
217  |  ALDH2  |  infer
348  |  APOE  |  infer
847  |  CAT  |  infer
1312  |  COMT  |  infer
1394  |  CRHR1  |  infer
1571  |  CYP2E1  |  infer
1812  |  DRD1  |  infer
1813  |  DRD2  |  infer
1814  |  DRD3  |  infer
1815  |  DRD4  |  infer
2554  |  GABRA1  |  infer
2559  |  GABRA6  |  infer
2560  |  GABRB1  |  infer
2561  |  GABRB2  |  infer
2566  |  GABRG2  |  infer
2904  |  GRIN2B  |  infer
2944  |  GSTM1  |  infer
3351  |  HTR1B  |  infer
3356  |  HTR2A  |  infer
3358  |  HTR2C  |  infer
3361  |  HTR5A  |  infer
3363  |  HTR7  |  infer
4128  |  MAOA  |  infer
4852  |  NPY  |  infer
1728  |  NQO1  |  infer
4835  |  NQO2  |  infer
4985  |  OPRD1  |  infer
4986  |  OPRK1  |  infer
4988  |  OPRM1  |  infer
5173  |  PDYN  |  infer
6506  |  SLC1A2  |  infer
6531  |  SLC6A3  |  infer
6532  |  SLC6A4  |  infer
6622  |  SNCA  |  infer
50833  |  TAS2R16  |  infer
5726  |  TAS2R38  |  infer
7124  |  TNF  |  infer
7166  |  TPH1  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:325)
100126791  |  EGOT  |  DISEASES
1080  |  CFTR  |  DISEASES
2554  |  GABRA1  |  DISEASES
50508  |  NOX3  |  DISEASES
55810  |  FOXJ2  |  DISEASES
7132  |  TNFRSF1A  |  DISEASES
1815  |  DRD4  |  DISEASES
51208  |  CLDN18  |  DISEASES
124  |  ADH1A  |  DISEASES
5714  |  PSMD8  |  DISEASES
112755  |  STX1B  |  DISEASES
2953  |  GSTT2  |  DISEASES
80339  |  PNPLA3  |  DISEASES
25828  |  TXN2  |  DISEASES
5173  |  PDYN  |  DISEASES
10627  |  MYL12A  |  DISEASES
479  |  ATP12A  |  DISEASES
4313  |  MMP2  |  DISEASES
2222  |  FDFT1  |  DISEASES
1666  |  DECR1  |  DISEASES
83988  |  NCALD  |  DISEASES
57030  |  SLC17A7  |  DISEASES
81576  |  CCDC130  |  DISEASES
2091  |  FBL  |  DISEASES
7040  |  TGFB1  |  DISEASES
973  |  CD79A  |  DISEASES
57817  |  HAMP  |  DISEASES
6347  |  CCL2  |  DISEASES
6346  |  CCL1  |  DISEASES
6688  |  SPI1  |  DISEASES
9896  |  FIG4  |  DISEASES
1839  |  HBEGF  |  DISEASES
9421  |  HAND1  |  DISEASES
338  |  APOB  |  DISEASES
5967  |  REG1A  |  DISEASES
4985  |  OPRD1  |  DISEASES
4317  |  MMP8  |  DISEASES
1958  |  EGR1  |  DISEASES
4852  |  NPY  |  DISEASES
2166  |  FAAH  |  DISEASES
2354  |  FOSB  |  DISEASES
7389  |  UROD  |  DISEASES
2678  |  GGT1  |  DISEASES
8484  |  GALR3  |  DISEASES
57053  |  CHRNA10  |  DISEASES
3630  |  INS  |  DISEASES
3040  |  HBA2  |  DISEASES
348  |  APOE  |  DISEASES
55821  |  ALLC  |  DISEASES
1571  |  CYP2E1  |  DISEASES
113  |  ADCY7  |  DISEASES
8864  |  PER2  |  DISEASES
51540  |  SCLY  |  DISEASES
1401  |  CRP  |  DISEASES
10526  |  IPO8  |  DISEASES
10677  |  AVIL  |  DISEASES
1593  |  CYP27A1  |  DISEASES
10643  |  IGF2BP3  |  DISEASES
3569  |  IL6  |  DISEASES
9177  |  HTR3B  |  DISEASES
3074  |  HEXB  |  DISEASES
6532  |  SLC6A4  |  DISEASES
217  |  ALDH2  |  DISEASES
1143  |  CHRNB4  |  DISEASES
23184  |  MESDC2  |  DISEASES
56052  |  ALG1  |  DISEASES
4969  |  OGN  |  DISEASES
495  |  ATP4A  |  DISEASES
5465  |  PPARA  |  DISEASES
25939  |  SAMHD1  |  DISEASES
5595  |  MAPK3  |  DISEASES
2033  |  EP300  |  DISEASES
2906  |  GRIN2D  |  DISEASES
3553  |  IL1B  |  DISEASES
84708  |  LNX1  |  DISEASES
1001  |  CDH3  |  DISEASES
2557  |  GABRA4  |  DISEASES
5443  |  POMC  |  DISEASES
5924  |  RASGRF2  |  DISEASES
127  |  ADH4  |  DISEASES
22937  |  SCAP  |  DISEASES
4986  |  OPRK1  |  DISEASES
51083  |  GAL  |  DISEASES
55749  |  CCAR1  |  DISEASES
56938  |  ARNTL2  |  DISEASES
51411  |  BIN2  |  DISEASES
64784  |  CRTC3  |  DISEASES
5373  |  PMM2  |  DISEASES
10351  |  ABCA8  |  DISEASES
432  |  ASGR1  |  DISEASES
7157  |  TP53  |  DISEASES
150094  |  SIK1  |  DISEASES
6531  |  SLC6A3  |  DISEASES
100996939  |  PYURF  |  DISEASES
2561  |  GABRB2  |  DISEASES
3358  |  HTR2C  |  DISEASES
1392  |  CRH  |  DISEASES
3439  |  IFNA1  |  DISEASES
6291  |  SAA4  |  DISEASES
6506  |  SLC1A2  |  DISEASES
2904  |  GRIN2B  |  DISEASES
7082  |  TJP1  |  DISEASES
5741  |  PTH  |  DISEASES
10413  |  YAP1  |  DISEASES
3087  |  HHEX  |  DISEASES
57630  |  SH3RF1  |  DISEASES
2890  |  GRIA1  |  DISEASES
10  |  NAT2  |  DISEASES
3361  |  HTR5A  |  DISEASES
3763  |  KCNJ6  |  DISEASES
653689  |  GSTT2B  |  DISEASES
1636  |  ACE  |  DISEASES
7109  |  TRAPPC10  |  DISEASES
3060  |  HCRT  |  DISEASES
27306  |  HPGDS  |  DISEASES
2565  |  GABRG1  |  DISEASES
2560  |  GABRB1  |  DISEASES
886  |  CCKAR  |  DISEASES
213  |  ALB  |  DISEASES
8820  |  HESX1  |  DISEASES
7349  |  UCN  |  DISEASES
128  |  ADH5  |  DISEASES
6690  |  SPINK1  |  DISEASES
9607  |  CARTPT  |  DISEASES
143872  |  ARHGAP42  |  DISEASES
5267  |  SERPINA4  |  DISEASES
1138  |  CHRNA5  |  DISEASES
5368  |  PNOC  |  DISEASES
5617  |  PRL  |  DISEASES
3479  |  IGF1  |  DISEASES
23440  |  OTP  |  DISEASES
7200  |  TRH  |  DISEASES
83660  |  TLN2  |  DISEASES
1140  |  CHRNB1  |  DISEASES
84342  |  COG8  |  DISEASES
9455  |  HOMER2  |  DISEASES
1816  |  DRD5  |  DISEASES
2915  |  GRM5  |  DISEASES
2353  |  FOS  |  DISEASES
125  |  ADH1B  |  DISEASES
255239  |  ANKK1  |  DISEASES
57099  |  AVEN  |  DISEASES
200558  |  APLF  |  DISEASES
2147  |  F2  |  DISEASES
5644  |  PRSS1  |  DISEASES
9575  |  CLOCK  |  DISEASES
4023  |  LPL  |  DISEASES
3265  |  HRAS  |  DISEASES
6868  |  ADAM17  |  DISEASES
836  |  CASP3  |  DISEASES
7368  |  UGT8  |  DISEASES
3952  |  LEP  |  DISEASES
55584  |  CHRNA9  |  DISEASES
55885  |  LMO3  |  DISEASES
1191  |  CLU  |  DISEASES
1136  |  CHRNA3  |  DISEASES
3350  |  HTR1A  |  DISEASES
1442  |  CSH1  |  DISEASES
9370  |  ADIPOQ  |  DISEASES
51085  |  MLXIPL  |  DISEASES
6863  |  TAC1  |  DISEASES
4018  |  LPA  |  DISEASES
9242  |  MSC  |  DISEASES
200539  |  ANKRD23  |  DISEASES
6014  |  RIT2  |  DISEASES
79075  |  DSCC1  |  DISEASES
23212  |  RRS1  |  DISEASES
3039  |  HBA1  |  DISEASES
386724  |  AMIGO3  |  DISEASES
1555  |  CYP2B6  |  DISEASES
154865  |  IQUB  |  DISEASES
1812  |  DRD1  |  DISEASES
121278  |  TPH2  |  DISEASES
29110  |  TBK1  |  DISEASES
64782  |  AEN  |  DISEASES
2903  |  GRIN2A  |  DISEASES
4887  |  NPY2R  |  DISEASES
10810  |  WASF3  |  DISEASES
51738  |  GHRL  |  DISEASES
342035  |  GLDN  |  DISEASES
885  |  CCK  |  DISEASES
4987  |  OPRL1  |  DISEASES
79658  |  ARHGAP10  |  DISEASES
1103  |  CHAT  |  DISEASES
3988  |  LIPA  |  DISEASES
57142  |  RTN4  |  DISEASES
1576  |  CYP3A4  |  DISEASES
3363  |  HTR7  |  DISEASES
7360  |  UGP2  |  DISEASES
4889  |  NPY5R  |  DISEASES
9639  |  ARHGEF10  |  DISEASES
4128  |  MAOA  |  DISEASES
4208  |  MEF2C  |  DISEASES
1395  |  CRHR2  |  DISEASES
113675  |  SDSL  |  DISEASES
3720  |  JARID2  |  DISEASES
1508  |  CTSB  |  DISEASES
7444  |  VRK2  |  DISEASES
3146  |  HMGB1  |  DISEASES
257101  |  ZNF683  |  DISEASES
8720  |  MBTPS1  |  DISEASES
6483  |  ST3GAL2  |  DISEASES
224  |  ALDH3A2  |  DISEASES
4205  |  MEF2A  |  DISEASES
50618  |  ITSN2  |  DISEASES
100506658  |  OCLN  |  DISEASES
3359  |  HTR3A  |  DISEASES
5265  |  SERPINA1  |  DISEASES
3240  |  HP  |  DISEASES
2555  |  GABRA2  |  DISEASES
781  |  CACNA2D1  |  DISEASES
2917  |  GRM7  |  DISEASES
7867  |  MAPKAPK3  |  DISEASES
841  |  CASP8  |  DISEASES
8936  |  WASF1  |  DISEASES
57016  |  AKR1B10  |  DISEASES
4151  |  MB  |  DISEASES
4638  |  MYLK  |  DISEASES
83666  |  PARP9  |  DISEASES
1002  |  CDH4  |  DISEASES
104  |  ADARB1  |  DISEASES
5646  |  PRSS3  |  DISEASES
1312  |  COMT  |  DISEASES
4886  |  NPY1R  |  DISEASES
10724  |  MGEA5  |  DISEASES
1813  |  DRD2  |  DISEASES
9937  |  DCLRE1A  |  DISEASES
2913  |  GRM3  |  DISEASES
27350  |  APOBEC3C  |  DISEASES
6000  |  RGS7  |  DISEASES
51022  |  GLRX2  |  DISEASES
336  |  APOA2  |  DISEASES
632  |  BGLAP  |  DISEASES
4121  |  MAN1A1  |  DISEASES
79626  |  TNFAIP8L2  |  DISEASES
246269  |  LACE1  |  DISEASES
1268  |  CNR1  |  DISEASES
3351  |  HTR1B  |  DISEASES
1137  |  CHRNA4  |  DISEASES
6658  |  SOX3  |  DISEASES
959  |  CD40LG  |  DISEASES
7803  |  PTP4A1  |  DISEASES
55277  |  FGGY  |  DISEASES
5146  |  PDE6C  |  DISEASES
8471  |  IRS4  |  DISEASES
79717  |  PPCS  |  DISEASES
80712  |  ESX1  |  DISEASES
27035  |  NOX1  |  DISEASES
129685  |  TAF8  |  DISEASES
2899  |  GRIK3  |  DISEASES
54577  |  UGT1A7  |  DISEASES
7099  |  TLR4  |  DISEASES
1269  |  CNR2  |  DISEASES
3376  |  IARS  |  DISEASES
11330  |  CTRC  |  DISEASES
6096  |  RORB  |  DISEASES
1325  |  CORT  |  DISEASES
219  |  ALDH1B1  |  DISEASES
83715  |  ESPN  |  DISEASES
11332  |  ACOT7  |  DISEASES
4129  |  MAOB  |  DISEASES
84912  |  SLC35B4  |  DISEASES
2563  |  GABRD  |  DISEASES
1536  |  CYBB  |  DISEASES
3356  |  HTR2A  |  DISEASES
22944  |  KIN  |  DISEASES
10455  |  ECI2  |  DISEASES
551  |  AVP  |  DISEASES
114131  |  UCN3  |  DISEASES
6462  |  SHBG  |  DISEASES
10087  |  COL4A3BP  |  DISEASES
5412  |  UBL3  |  DISEASES
8777  |  MPDZ  |  DISEASES
5268  |  SERPINB5  |  DISEASES
1814  |  DRD3  |  DISEASES
4336  |  MOBP  |  DISEASES
9467  |  SH3BP5  |  DISEASES
2617  |  GARS  |  DISEASES
1443  |  CSH2  |  DISEASES
1621  |  DBH  |  DISEASES
130  |  ADH6  |  DISEASES
2875  |  GPT  |  DISEASES
2912  |  GRM2  |  DISEASES
174  |  AFP  |  DISEASES
27327  |  TNRC6A  |  DISEASES
6489  |  ST8SIA1  |  DISEASES
23426  |  GRIP1  |  DISEASES
594857  |  NPS  |  DISEASES
1394  |  CRHR1  |  DISEASES
221037  |  JMJD1C  |  DISEASES
25780  |  RASGRP3  |  DISEASES
7122  |  CLDN5  |  DISEASES
1135  |  CHRNA2  |  DISEASES
728441  |  GGT2  |  DISEASES
164668  |  APOBEC3H  |  DISEASES
7018  |  TF  |  DISEASES
210  |  ALAD  |  DISEASES
3267  |  AGFG1  |  DISEASES
2641  |  GCG  |  DISEASES
1385  |  CREB1  |  DISEASES
6916  |  TBXAS1  |  DISEASES
389158  |  PLSCR5  |  DISEASES
4988  |  OPRM1  |  DISEASES
10163  |  WASF2  |  DISEASES
7124  |  TNF  |  DISEASES
26054  |  SENP6  |  DISEASES
7086  |  TKT  |  DISEASES
139728  |  PNCK  |  DISEASES
2566  |  GABRG2  |  DISEASES
10015  |  PDCD6IP  |  DISEASES
3586  |  IL10  |  DISEASES
627  |  BDNF  |  DISEASES
3077  |  HFE  |  DISEASES
131  |  ADH7  |  DISEASES
114907  |  FBXO32  |  DISEASES
23025  |  UNC13A  |  DISEASES
5715  |  PSMD9  |  DISEASES
3684  |  ITGAM  |  DISEASES
136541  |  PRSS58  |  DISEASES
64786  |  TBC1D15  |  DISEASES
8742  |  TNFSF12  |  DISEASES
391104  |  VHLL  |  DISEASES
8677  |  STX10  |  DISEASES
284424  |  MIR7-3HG  |  DISEASES
378805  |  LINC-PINT  |  DISEASES
Locus(Waiting for update.)
Disease ID 1817
Disease alcohol abuse
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:65)
HP:0001394  |  Hepatic cirrhosis  |  16
HP:0001733  |  Pancreatic inflammation  |  12
HP:0000716  |  Depression  |  8
HP:0000739  |  Anxiety  |  8
HP:0001397  |  Hepatic steatosis  |  7
HP:0012115  |  Liver inflammation  |  5
HP:0000822  |  Hypertension  |  5
HP:0000708  |  Behavioral problems  |  5
HP:0001735  |  Acute pancreatitis  |  4
HP:0100033  |  Tic disorder  |  3
HP:0007302  |  Bipolar disorder  |  3
HP:0001298  |  Encephalopathy  |  3
HP:0100753  |  Schizophrenia  |  3
HP:0000726  |  Dementia  |  3
HP:0002664  |  Neoplasia  |  3
HP:0002360  |  Sleep disturbance  |  2
HP:0012531  |  Pain  |  2
HP:0001513  |  Obesity  |  2
HP:0012075  |  Personality disorder  |  2
HP:0000718  |  Aggressive behaviour  |  2
HP:0006280  |  Chronic pancreas inflammation  |  2
HP:0000505  |  Poor vision  |  2
HP:0002480  |  Hepatic encephalopathy  |  2
HP:0000939  |  Osteoporosis  |  2
HP:0000670  |  Dental caries  |  2
HP:0001297  |  Cerebral vascular events  |  2
HP:0002591  |  Voracious appetite  |  1
HP:0001635  |  Congestive heart failure  |  1
HP:0003077  |  Hyperlipidemia  |  1
HP:0011675  |  Arrhythmias  |  1
HP:0000734  |  Disinhibition  |  1
HP:0001410  |  Decreased liver function  |  1
HP:0002529  |  Neuronal loss in central nervous system  |  1
HP:0001873  |  Low platelet count  |  1
HP:0000952  |  Yellow skin  |  1
HP:0000855  |  Insulin resistance  |  1
HP:0000709  |  Psychosis  |  1
HP:0007185  |  Loss of consciousness  |  1
HP:0001638  |  Cardiomyopathy  |  1
HP:0001289  |  Confusion  |  1
HP:0000737  |  Irritability  |  1
HP:0100806  |  Sepsis  |  1
HP:0002719  |  infections, recurrent  |  1
HP:0001300  |  Parkinsonism  |  1
HP:0100543  |  Cognitive deficits  |  1
HP:0001644  |  Congestive cardiomyopathy  |  1
HP:0004395  |  Malnutrition  |  1
HP:0200123  |  Chronic liver inflammation  |  1
HP:0000819  |  Diabetes mellitus  |  1
HP:0012393  |  Allergy  |  1
HP:0003201  |  Rhabdomyolysis  |  1
HP:0001251  |  Ataxia  |  1
HP:0000821  |  Underactive thyroid  |  1
HP:0001402  |  Hepatocellular carcinoma  |  1
HP:0002180  |  Neurodegeneration  |  1
HP:0001645  |  Sudden cardiac death  |  1
HP:0002354  |  Memory loss  |  1
HP:0100507  |  Folate deficiency  |  1
HP:0002090  |  Pneumonia  |  1
HP:0012664  |  Reduced ejection fraction  |  1
HP:0011110  |  Inflammation of tonsils  |  1
HP:0005263  |  Gastritis  |  1
HP:0000010  |  Frequent urinary tract infections  |  1
HP:0000989  |  pruritis  |  1
HP:0030731  |  Carcinoma  |  1
Disease ID 1817
Disease alcohol abuse
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:23)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs12299842191740910327AKR1A1umls:C0085762BeFreeAmong conventional markers of alcohol abuse, the mean corpuscular volume (MCV) of erythrocytes is prognostic of alcohol-related cancer and its predictivity increases when combined with functional polymorphisms of alcohol dehydrogenase (ADH1B [rs1229984] and ADH1C [rs698]) and the mitochondrial aldehyde dehydrogenase (ALDH2 [rs671]).0.0010857672012ADH1B499318162TC
rs122998424553426125ADH1Bumls:C0085762BeFreeWe genotyped the rs1229984 G→A variant of the alcohol dehydrogenase 1B (ADH1B) gene, which is associated with lower prevalence of alcohol abuse and dependence.0.0255704132014ADH1B499318162TC
rs122998421917409125ADH1Bumls:C0085762BeFreeAmong conventional markers of alcohol abuse, the mean corpuscular volume (MCV) of erythrocytes is prognostic of alcohol-related cancer and its predictivity increases when combined with functional polymorphisms of alcohol dehydrogenase (ADH1B [rs1229984] and ADH1C [rs698]) and the mitochondrial aldehyde dehydrogenase (ALDH2 [rs671]).0.0255704132012ADH1B499318162TC
rs122998421917409217ALDH2umls:C0085762BeFreeAmong conventional markers of alcohol abuse, the mean corpuscular volume (MCV) of erythrocytes is prognostic of alcohol-related cancer and its predictivity increases when combined with functional polymorphisms of alcohol dehydrogenase (ADH1B [rs1229984] and ADH1C [rs698]) and the mitochondrial aldehyde dehydrogenase (ALDH2 [rs671]).0.0276660032012ADH1B499318162TC
rs122998421917409126ADH1Cumls:C0085762BeFreeAmong conventional markers of alcohol abuse, the mean corpuscular volume (MCV) of erythrocytes is prognostic of alcohol-related cancer and its predictivity increases when combined with functional polymorphisms of alcohol dehydrogenase (ADH1B [rs1229984] and ADH1C [rs698]) and the mitochondrial aldehyde dehydrogenase (ALDH2 [rs671]).0.0126494862012ADH1B499318162TC
rs122998424018899125ADH1Bumls:C0085762BeFreeGiven the logistic and ethical constraints that would be associated with a trial of alcohol use to prevent depression, we aimed to complete a Mendelian randomization study to determine if a genetic polymorphism associated with alcohol abuse and dependence (ADH1B rs1229984 G-->A) contributed to modulate the risk of depression in a community-derived cohort of older men.0.0255704132013ADH1B499318162TC
rs1711074724491795121278TPH2umls:C0085762BeFreeMore specifically, we observed that the T allele in the rs4570625 polymorphism was associated with psychotic disorders, and the A allele in the rs17110747 TPH2 polymorphism was associated with alcohol abuse in patients with TLE.0.0002714422014TPH21272032174GA
rs1800562261644933077HFEumls:C0085762BeFreeIn Caucasians, C282Y HFE homozygotes are numerous, but they are only predisposed to hemochromatosis; complete organ disease develops in a minority, due to alcohol abuse or concurrent genetic modifiers that are now being identified.0.0008143262015HFE626092913GA
rs1800562205420383077HFEumls:C0085762BeFreeUnlike these rare instances, in white people, homozygotes for C282Y polymorphism in HFE are numerous, but they are only predisposed to hemochromatosis; complete organ disease develops in a minority, when these individuals abuse alcohol or from other unidentified modifying factors.0.0008143262010HFE626092913GA
rs23060732253839856938ARNTL2umls:C0085762BeFreeConcerning anxiety disorders and alcohol use disorders, the current findings are preliminary and need further verification to explain the association of ARNTL2, being suggestive only, with social phobia (rs2306073) and with alcohol abuse (rs7958822, rs4964057).0.0005428842012ARNTL2;ARNTL2-AS11227402904CT
rs457062524491795121278TPH2umls:C0085762BeFreeMore specifically, we observed that the T allele in the rs4570625 polymorphism was associated with psychotic disorders, and the A allele in the rs17110747 TPH2 polymorphism was associated with alcohol abuse in patients with TLE.0.0002714422014TPH21271938143GT
rs49640572055469456938ARNTL2umls:C0085762BeFreeARNTL2 GT haplotype (rs7958822-rs4964057) associated suggestively with alcohol abuse diagnosis (P = 0.0013).0.0005428842010ARNTL21227363909TG
rs49640572253839856938ARNTL2umls:C0085762BeFreeConcerning anxiety disorders and alcohol use disorders, the current findings are preliminary and need further verification to explain the association of ARNTL2, being suggestive only, with social phobia (rs2306073) and with alcohol abuse (rs7958822, rs4964057).0.0005428842012ARNTL21227363909TG
rs6712191740910327AKR1A1umls:C0085762BeFreeAmong conventional markers of alcohol abuse, the mean corpuscular volume (MCV) of erythrocytes is prognostic of alcohol-related cancer and its predictivity increases when combined with functional polymorphisms of alcohol dehydrogenase (ADH1B [rs1229984] and ADH1C [rs698]) and the mitochondrial aldehyde dehydrogenase (ALDH2 [rs671]).0.0010857672012ALDH212111803962GA
rs67121917409126ADH1Cumls:C0085762BeFreeAmong conventional markers of alcohol abuse, the mean corpuscular volume (MCV) of erythrocytes is prognostic of alcohol-related cancer and its predictivity increases when combined with functional polymorphisms of alcohol dehydrogenase (ADH1B [rs1229984] and ADH1C [rs698]) and the mitochondrial aldehyde dehydrogenase (ALDH2 [rs671]).0.0126494862012ALDH212111803962GA
rs67121917409217ALDH2umls:C0085762BeFreeAmong conventional markers of alcohol abuse, the mean corpuscular volume (MCV) of erythrocytes is prognostic of alcohol-related cancer and its predictivity increases when combined with functional polymorphisms of alcohol dehydrogenase (ADH1B [rs1229984] and ADH1C [rs698]) and the mitochondrial aldehyde dehydrogenase (ALDH2 [rs671]).0.0276660032012ALDH212111803962GA
rs67121917409125ADH1Bumls:C0085762BeFreeAmong conventional markers of alcohol abuse, the mean corpuscular volume (MCV) of erythrocytes is prognostic of alcohol-related cancer and its predictivity increases when combined with functional polymorphisms of alcohol dehydrogenase (ADH1B [rs1229984] and ADH1C [rs698]) and the mitochondrial aldehyde dehydrogenase (ALDH2 [rs671]).0.0255704132012ALDH212111803962GA
rs69821917409217ALDH2umls:C0085762BeFreeAmong conventional markers of alcohol abuse, the mean corpuscular volume (MCV) of erythrocytes is prognostic of alcohol-related cancer and its predictivity increases when combined with functional polymorphisms of alcohol dehydrogenase (ADH1B [rs1229984] and ADH1C [rs698]) and the mitochondrial aldehyde dehydrogenase (ALDH2 [rs671]).0.0276660032012ADH1C499339632TC,A
rs69821917409125ADH1Bumls:C0085762BeFreeAmong conventional markers of alcohol abuse, the mean corpuscular volume (MCV) of erythrocytes is prognostic of alcohol-related cancer and its predictivity increases when combined with functional polymorphisms of alcohol dehydrogenase (ADH1B [rs1229984] and ADH1C [rs698]) and the mitochondrial aldehyde dehydrogenase (ALDH2 [rs671]).0.0255704132012ADH1C499339632TC,A
rs6982191740910327AKR1A1umls:C0085762BeFreeAmong conventional markers of alcohol abuse, the mean corpuscular volume (MCV) of erythrocytes is prognostic of alcohol-related cancer and its predictivity increases when combined with functional polymorphisms of alcohol dehydrogenase (ADH1B [rs1229984] and ADH1C [rs698]) and the mitochondrial aldehyde dehydrogenase (ALDH2 [rs671]).0.0010857672012ADH1C499339632TC,A
rs69821917409126ADH1Cumls:C0085762BeFreeAmong conventional markers of alcohol abuse, the mean corpuscular volume (MCV) of erythrocytes is prognostic of alcohol-related cancer and its predictivity increases when combined with functional polymorphisms of alcohol dehydrogenase (ADH1B [rs1229984] and ADH1C [rs698]) and the mitochondrial aldehyde dehydrogenase (ALDH2 [rs671]).0.0126494862012ADH1C499339632TC,A
rs79588222253839856938ARNTL2umls:C0085762BeFreeConcerning anxiety disorders and alcohol use disorders, the current findings are preliminary and need further verification to explain the association of ARNTL2, being suggestive only, with social phobia (rs2306073) and with alcohol abuse (rs7958822, rs4964057).0.0005428842012ARNTL21227348173GA
rs79588222055469456938ARNTL2umls:C0085762BeFreeARNTL2 GT haplotype (rs7958822-rs4964057) associated suggestively with alcohol abuse diagnosis (P = 0.0013).0.0005428842010ARNTL21227348173GA
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:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)