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Pediatric Disease Annotations & Medicines



   anorexia nervosa
  

Disease ID 531
Disease anorexia nervosa
Definition
An eating disorder that is characterized by the lack or loss of APPETITE, known as ANOREXIA. Other features include excess fear of becoming OVERWEIGHT; BODY IMAGE disturbance; significant WEIGHT LOSS; refusal to maintain minimal normal weight; and AMENORRHEA. This disorder occurs most frequently in adolescent females. (APA, Thesaurus of Psychological Index Terms, 1994)
Synonym
an - anorexia nervosa
anorexia mentalis
anorexia nervosa (disorder)
anorexia nervosa [disease/finding]
anorexia nervosas
anorexia, nervosa
nervosa, anorexia
nervosas, anorexia
DOID
UMLS
C0003125
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:86)
C0162429  |  malnourished  |  12
C0013473  |  eating disorder  |  11
C0002453  |  amenorrhea  |  6
C0003467  |  anxiety  |  6
C0162429  |  malnutrition  |  5
C0029456  |  osteoporosis  |  5
C0006370  |  bulimia  |  3
C0002871  |  anemia  |  2
C0005940  |  bone disease  |  2
C0679466  |  cognitive deficits  |  2
C0162429  |  undernutrition  |  2
C0032326  |  pneumothorax  |  2
C0030305  |  pancreatitis  |  2
C0013473  |  eating disorders  |  2
C0002020  |  alexithymia  |  2
C0011570  |  depression  |  2
C0027051  |  myocardial infarct  |  2
C2267227  |  bulimia nervosa  |  2
C0027051  |  myocardial infarction  |  2
C0035078  |  renal failure  |  1
C0022116  |  ischemia  |  1
C0003615  |  appendicitis  |  1
C0022735  |  klinefelter syndrome  |  1
C0003469  |  anxiety disorder  |  1
C0007222  |  cardiovascular disorders  |  1
C0001627  |  congenital adrenal hyperplasia  |  1
C0013990  |  emphysema  |  1
C0042373  |  vascular disorder  |  1
C0007104  |  female breast cancer  |  1
C0206734  |  hemangioblastoma  |  1
C0006625  |  cachexia  |  1
C0020598  |  hypoglycemia  |  1
C0019158  |  hepatitis  |  1
C0034888  |  rectal prolapse  |  1
C0011854  |  type 1 diabetes  |  1
C0878544  |  cardiomyopathy  |  1
C0162429  |  underfed  |  1
C0001197  |  acrodermatitis  |  1
C0011880  |  diabetic ketoacidosis  |  1
C0017178  |  gastrointestinal disorder  |  1
C0221036  |  acrodermatitis enteropathica  |  1
C0598639  |  hypercortisolemia  |  1
C0003469  |  anxiety disorders  |  1
C0001339  |  acute pancreatitis  |  1
C0038353  |  gastric dilatation  |  1
C0018802  |  congestive heart failure  |  1
C0007177  |  cardiac tamponade  |  1
C0010346  |  crohn's disease  |  1
C0043121  |  wernicke's encephalopathy  |  1
C0031154  |  peritonitis  |  1
C0017178  |  gastrointestinal disorders  |  1
C0034063  |  pulmonary edema  |  1
C0442874  |  neuropathy  |  1
C0042373  |  vascular disease  |  1
C0031117  |  peripheral neuropathy  |  1
C0014848  |  achalasia  |  1
C0033975  |  psychosis  |  1
C0008350  |  gallstones  |  1
C0006012  |  borderline personality disorder  |  1
C0022658  |  nephropathy  |  1
C0011847  |  diabetes  |  1
C0038828  |  superior mesenteric artery syndrome  |  1
C0038436  |  post-traumatic stress disorder  |  1
C0006142  |  breast cancer  |  1
C0086588  |  marasmus  |  1
C0236792  |  asperger syndrome  |  1
C0007570  |  celiac disease  |  1
C0018801  |  heart failure  |  1
C0020617  |  hypoglycemic coma  |  1
C0238033  |  male breast cancer  |  1
C0042373  |  vascular disorders  |  1
C0004763  |  barrett's esophagus  |  1
C0042769  |  virus infection  |  1
C0025202  |  melanoma  |  1
C0011849  |  diabetes mellitus  |  1
C1258215  |  ileus  |  1
C0020459  |  hyperinsulinaemia  |  1
C0020459  |  hyperinsulinemia  |  1
C0012739  |  disseminated intravascular coagulation  |  1
C0699893  |  non-melanoma skin cancer  |  1
C0011854  |  type 1 diabetes mellitus  |  1
C0028756  |  morbid obesity  |  1
C1621895  |  adrenal hyperplasia  |  1
C0038436  |  posttraumatic stress disorder  |  1
C0155626  |  acute myocardial infarction  |  1
C0023530  |  leukopenia  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:3)
HTR2A  |  3356  |  CTD_human
BDNF  |  627  |  CTD_human
SOX2-OT  |  347689  |  GWASCAT
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:42)
181  |  AGRP  |  infer
9472  |  AKAP6  |  infer
421  |  ARVCF  |  infer
627  |  BDNF  |  infer
1268  |  CNR1  |  infer
1312  |  COMT  |  infer
1813  |  DRD2  |  infer
1814  |  DRD3  |  infer
2099  |  ESR1  |  infer
2100  |  ESR2  |  infer
2119  |  ETV5  |  infer
2166  |  FAAH  |  infer
728215  |  FAM155A  |  infer
79068  |  FTO  |  infer
51738  |  GHRL  |  infer
132789  |  GNPDA2  |  infer
3352  |  HTR1D  |  infer
3356  |  HTR2A  |  infer
3777  |  KCNK3  |  infer
3782  |  KCNN3  |  infer
79047  |  KCTD15  |  infer
4036  |  LRP2  |  infer
4160  |  MC4R  |  infer
11343  |  MGLL  |  infer
23788  |  MTCH2  |  infer
27163  |  NAAA  |  infer
257194  |  NEGR1  |  infer
22854  |  NTNG1  |  infer
4985  |  OPRD1  |  infer
128756  |  RPL15P1  |  infer
25970  |  SH2B1  |  infer
6530  |  SLC6A2  |  infer
6532  |  SLC6A4  |  infer
23635  |  SSBP2  |  infer
129787  |  TMEM18  |  infer
7124  |  TNF  |  infer
7126  |  TNFAIP1  |  infer
7351  |  UCP2  |  infer
7352  |  UCP3  |  infer
9686  |  VGLL4  |  infer
219578  |  ZNF804B  |  infer
128153  |  SPATA17  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:208)
100130776  |  AGAP2-AS1  |  DISEASES
2101  |  ESRRA  |  DISEASES
1815  |  DRD4  |  DISEASES
80863  |  PRRT1  |  DISEASES
10454  |  TAB1  |  DISEASES
5173  |  PDYN  |  DISEASES
5020  |  OXT  |  DISEASES
6530  |  SLC6A2  |  DISEASES
30844  |  EHD4  |  DISEASES
56729  |  RETN  |  DISEASES
6822  |  SULT2A1  |  DISEASES
26291  |  FGF21  |  DISEASES
51200  |  CPA4  |  DISEASES
10135  |  NAMPT  |  DISEASES
5539  |  PPY  |  DISEASES
2690  |  GHR  |  DISEASES
1007  |  CDH9  |  DISEASES
2908  |  NR3C1  |  DISEASES
338  |  APOB  |  DISEASES
83444  |  INO80B  |  DISEASES
3485  |  IGFBP2  |  DISEASES
4985  |  OPRD1  |  DISEASES
7276  |  TTR  |  DISEASES
9519  |  TBPL1  |  DISEASES
2691  |  GHRH  |  DISEASES
8600  |  TNFSF11  |  DISEASES
3375  |  IAPP  |  DISEASES
80218  |  NAA50  |  DISEASES
2693  |  GHSR  |  DISEASES
4852  |  NPY  |  DISEASES
1271  |  CNTFR  |  DISEASES
2166  |  FAAH  |  DISEASES
4159  |  MC3R  |  DISEASES
3630  |  INS  |  DISEASES
1890  |  TYMP  |  DISEASES
83854  |  ANGPTL6  |  DISEASES
51540  |  SCLY  |  DISEASES
6117  |  RPA1  |  DISEASES
1401  |  CRP  |  DISEASES
80896  |  NPL  |  DISEASES
1593  |  CYP27A1  |  DISEASES
79074  |  C2orf49  |  DISEASES
3569  |  IL6  |  DISEASES
9177  |  HTR3B  |  DISEASES
51103  |  NDUFAF1  |  DISEASES
6532  |  SLC6A4  |  DISEASES
2901  |  GRIK5  |  DISEASES
421  |  ARVCF  |  DISEASES
3553  |  IL1B  |  DISEASES
7301  |  TYRO3  |  DISEASES
2892  |  GRIA3  |  DISEASES
5443  |  POMC  |  DISEASES
80321  |  CEP70  |  DISEASES
10512  |  SEMA3C  |  DISEASES
51083  |  GAL  |  DISEASES
5286  |  PIK3C2A  |  DISEASES
3782  |  KCNN3  |  DISEASES
5972  |  REN  |  DISEASES
3484  |  IGFBP1  |  DISEASES
3358  |  HTR2C  |  DISEASES
6570  |  SLC18A1  |  DISEASES
2796  |  GNRH1  |  DISEASES
1392  |  CRH  |  DISEASES
4915  |  NTRK2  |  DISEASES
53942  |  CNTN5  |  DISEASES
9472  |  AKAP6  |  DISEASES
5741  |  PTH  |  DISEASES
3192  |  HNRNPU  |  DISEASES
6750  |  SST  |  DISEASES
10417  |  SPON2  |  DISEASES
181  |  AGRP  |  DISEASES
3060  |  HCRT  |  DISEASES
81570  |  CLPB  |  DISEASES
213  |  ALB  |  DISEASES
1359  |  CPA3  |  DISEASES
7349  |  UCN  |  DISEASES
4982  |  TNFRSF11B  |  DISEASES
136242  |  PRSS37  |  DISEASES
11067  |  C10orf10  |  DISEASES
552  |  AVPR1A  |  DISEASES
4160  |  MC4R  |  DISEASES
4909  |  NTF4  |  DISEASES
50964  |  SOST  |  DISEASES
4054  |  LTBP3  |  DISEASES
5617  |  PRL  |  DISEASES
3479  |  IGF1  |  DISEASES
7200  |  TRH  |  DISEASES
11280  |  SCN11A  |  DISEASES
55790  |  CSGALNACT1  |  DISEASES
57493  |  HEG1  |  DISEASES
7351  |  UCP2  |  DISEASES
3952  |  LEP  |  DISEASES
2688  |  GH1  |  DISEASES
3352  |  HTR1D  |  DISEASES
619373  |  MBOAT4  |  DISEASES
3350  |  HTR1A  |  DISEASES
9370  |  ADIPOQ  |  DISEASES
119682  |  OR51L1  |  DISEASES
6181  |  RPLP2  |  DISEASES
1879  |  EBF1  |  DISEASES
55600  |  ITLN1  |  DISEASES
7352  |  UCP3  |  DISEASES
5021  |  OXTR  |  DISEASES
8227  |  AKAP17A  |  DISEASES
2863  |  GPR39  |  DISEASES
284359  |  IZUMO1  |  DISEASES
121278  |  TPH2  |  DISEASES
219578  |  ZNF804B  |  DISEASES
3953  |  LEPR  |  DISEASES
277  |  AMY1B  |  DISEASES
1675  |  CFD  |  DISEASES
91624  |  NEXN  |  DISEASES
353288  |  KRT26  |  DISEASES
51738  |  GHRL  |  DISEASES
885  |  CCK  |  DISEASES
57142  |  RTN4  |  DISEASES
3363  |  HTR7  |  DISEASES
4889  |  NPY5R  |  DISEASES
8788  |  DLK1  |  DISEASES
4128  |  MAOA  |  DISEASES
1395  |  CRHR2  |  DISEASES
51094  |  ADIPOR1  |  DISEASES
27255  |  CNTN6  |  DISEASES
145264  |  SERPINA12  |  DISEASES
55179  |  FAIM  |  DISEASES
866  |  SERPINA6  |  DISEASES
2100  |  ESR2  |  DISEASES
10950  |  BTG3  |  DISEASES
10617  |  STAMBP  |  DISEASES
347148  |  QRFP  |  DISEASES
2879  |  GPX4  |  DISEASES
50618  |  ITSN2  |  DISEASES
4983  |  OPHN1  |  DISEASES
3359  |  HTR3A  |  DISEASES
2695  |  GIP  |  DISEASES
93034  |  NT5C1B  |  DISEASES
127343  |  DMBX1  |  DISEASES
5697  |  PYY  |  DISEASES
1312  |  COMT  |  DISEASES
4860  |  PNP  |  DISEASES
1813  |  DRD2  |  DISEASES
128153  |  SPATA17  |  DISEASES
343035  |  RD3  |  DISEASES
3664  |  IRF6  |  DISEASES
3814  |  KISS1  |  DISEASES
7432  |  VIP  |  DISEASES
632  |  BGLAP  |  DISEASES
253738  |  EBF3  |  DISEASES
8732  |  RNGTT  |  DISEASES
1268  |  CNR1  |  DISEASES
3351  |  HTR1B  |  DISEASES
22854  |  NTNG1  |  DISEASES
278  |  AMY1C  |  DISEASES
276  |  AMY1A  |  DISEASES
988  |  CDC5L  |  DISEASES
129685  |  TAF8  |  DISEASES
252995  |  FNDC5  |  DISEASES
2170  |  FABP3  |  DISEASES
7321  |  UBE2D1  |  DISEASES
6048  |  RNF5  |  DISEASES
4879  |  NPPB  |  DISEASES
4878  |  NPPA  |  DISEASES
114798  |  SLITRK1  |  DISEASES
3356  |  HTR2A  |  DISEASES
56261  |  GPCPD1  |  DISEASES
5080  |  PAX6  |  DISEASES
9365  |  KL  |  DISEASES
551  |  AVP  |  DISEASES
119679  |  OR52J3  |  DISEASES
401667  |  OR51A2  |  DISEASES
401666  |  OR51A4  |  DISEASES
8544  |  PIR  |  DISEASES
6462  |  SHBG  |  DISEASES
3486  |  IGFBP3  |  DISEASES
293  |  SLC25A6  |  DISEASES
51761  |  ATP8A2  |  DISEASES
1814  |  DRD3  |  DISEASES
5901  |  RAN  |  DISEASES
9244  |  CRLF1  |  DISEASES
55188  |  RIC8B  |  DISEASES
145270  |  PRIMA1  |  DISEASES
84628  |  NTNG2  |  DISEASES
6152  |  RPL24  |  DISEASES
152330  |  CNTN4  |  DISEASES
594857  |  NPS  |  DISEASES
1394  |  CRHR1  |  DISEASES
7018  |  TF  |  DISEASES
79843  |  FAM124B  |  DISEASES
22891  |  ZNF365  |  DISEASES
176  |  ACAN  |  DISEASES
2641  |  GCG  |  DISEASES
3481  |  IGF2  |  DISEASES
94122  |  SYTL5  |  DISEASES
7124  |  TNF  |  DISEASES
65065  |  NBEAL1  |  DISEASES
9686  |  VGLL4  |  DISEASES
55074  |  OXR1  |  DISEASES
79897  |  RPP21  |  DISEASES
627  |  BDNF  |  DISEASES
3483  |  IGFALS  |  DISEASES
64641  |  EBF2  |  DISEASES
2053  |  EPHX2  |  DISEASES
4925  |  NUCB2  |  DISEASES
64426  |  SUDS3  |  DISEASES
5726  |  TAS2R38  |  DISEASES
23601  |  CLEC5A  |  DISEASES
64493  |  LINC00235  |  DISEASES
347689  |  SOX2-OT  |  DISEASES
Locus(Waiting for update.)
Disease ID 531
Disease anorexia nervosa
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:87)
HP:0000141  |  Abnormal absence of menstruation  |  6
HP:0000739  |  Anxiety  |  6
HP:0004395  |  Malnutrition  |  5
HP:0000939  |  Osteoporosis  |  5
HP:0001824  |  Weight loss  |  4
HP:0100543  |  Cognitive deficits  |  4
HP:0000752  |  Hyperactive behavior  |  4
HP:0004325  |  Low body weight  |  3
HP:0002015  |  Swallowing difficulty  |  3
HP:0100739  |  Binge and purge  |  3
HP:0000708  |  Behavioral problems  |  2
HP:0002107  |  Collapsed lung  |  2
HP:0001658  |  Myocardial infarction  |  2
HP:0011675  |  Arrhythmias  |  2
HP:0001259  |  Coma  |  2
HP:0000716  |  Depression  |  2
HP:0200136  |  Oral-pharyngeal dysphagia  |  2
HP:0001410  |  Decreased liver function  |  2
HP:0001733  |  Pancreatic inflammation  |  2
HP:0012531  |  Pain  |  2
HP:0002013  |  Emesis  |  2
HP:0001662  |  Bradycardia  |  2
HP:0001903  |  Anemia  |  2
HP:0000112  |  Nephropathy  |  1
HP:0001882  |  Decreased blood leukocyte number  |  1
HP:0002035  |  Rectal prolapse  |  1
HP:0100280  |  Morbus Crohn  |  1
HP:0008258  |  Congenital adrenal hyperplasia  |  1
HP:0001518  |  Small for gestational age  |  1
HP:0012076  |  Borderline personality disorder  |  1
HP:0001638  |  Cardiomyopathy  |  1
HP:0000938  |  Decreased bone mineral density  |  1
HP:0100580  |  Barrett's esophagus  |  1
HP:0002459  |  Dysautonomia  |  1
HP:0001325  |  Coma caused by low blood sugar  |  1
HP:0001250  |  Seizures  |  1
HP:0001941  |  acidemia  |  1
HP:0002861  |  Melanoma  |  1
HP:0000969  |  Dropsy  |  1
HP:0002902  |  Hyponatremia  |  1
HP:0000711  |  Restlessness  |  1
HP:0012075  |  Personality disorder  |  1
HP:0001953  |  Diabetic ketosis  |  1
HP:0010797  |  Hemangioblastoma  |  1
HP:0010677  |  Enuresis nocturna  |  1
HP:0008770  |  Obsessive-compulsive trait  |  1
HP:0002500  |  Leukoaraiosis  |  1
HP:0002148  |  Hypophosphataemia  |  1
HP:0001298  |  Encephalopathy  |  1
HP:0000805  |  Enuresis  |  1
HP:0000842  |  Elevated insulin level  |  1
HP:0001664  |  Torsade de pointes  |  1
HP:0001943  |  Hypoglycemia  |  1
HP:0012115  |  Liver inflammation  |  1
HP:0001993  |  Ketoacidosis  |  1
HP:0000083  |  Renal insufficiency  |  1
HP:0002595  |  Gastrointestinal atony  |  1
HP:0000858  |  Menstrual irregularity  |  1
HP:0003002  |  Breast carcinoma  |  1
HP:0002918  |  High blood magnesium levels  |  1
HP:0100598  |  Pulmonary oedema  |  1
HP:0000786  |  Primary amenorrhea  |  1
HP:0003281  |  Increased ferritin  |  1
HP:0001631  |  Atria septal defect  |  1
HP:0000709  |  Psychosis  |  1
HP:0000718  |  Aggressive behaviour  |  1
HP:0001081  |  Gallstones  |  1
HP:0010783  |  Erythema  |  1
HP:0002097  |  Pulmonary emphysema  |  1
HP:0002608  |  Celiac disease  |  1
HP:0005972  |  Respiratory acidosis  |  1
HP:0004326  |  Cachexia  |  1
HP:0002900  |  Hypokalemia  |  1
HP:0001944  |  Dehydration  |  1
HP:0005521  |  Disseminated intravascular coagulation  |  1
HP:0002647  |  Aortic dissection  |  1
HP:0008221  |  Enlarged adrenal glands  |  1
HP:0001735  |  Acute pancreatitis  |  1
HP:0000572  |  Visual loss  |  1
HP:0002045  |  Abnormally low body temperature  |  1
HP:0001635  |  Congestive heart failure  |  1
HP:0005110  |  Atrial fibrillation  |  1
HP:0002586  |  Peritonitis  |  1
HP:0100962  |  Shyness  |  1
HP:0009830  |  Peripheral neuritis  |  1
HP:0002575  |  Tracheoesophageal fistula  |  1
HP:0002571  |  Achalasia  |  1
Disease ID 531
Disease anorexia nervosa
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:44)
C0013473  |  eating disorder  |  9
C0003467  |  anxiety  |  6
C0002453  |  amenorrhea  |  6
C0029456  |  osteoporosis  |  5
C0815110  |  perfectionism  |  5
C0162429  |  malnutrition  |  5
C0871381  |  social cognition  |  3
C0277787  |  stigma  |  3
C0175696  |  g syndrome  |  3
C0006370  |  bulimia  |  3
C0860549  |  refeeding syndrome  |  3
C0013473  |  eating disorders  |  2
C0311276  |  severe malnutrition  |  2
C0679466  |  cognitive deficits  |  2
C0042963  |  vomiting  |  2
C0032326  |  pneumothorax  |  2
C0011570  |  depression  |  2
C0002020  |  alexithymia  |  2
C0006625  |  cachexia  |  1
C0020672  |  hypothermia  |  1
C0878544  |  cardiomyopathy  |  1
C0221036  |  acrodermatitis enteropathica  |  1
C1393529  |  vascular complications  |  1
C0231303  |  distress  |  1
C0018801  |  heart failure  |  1
C0020625  |  hyponatremia  |  1
C0033975  |  psychosis  |  1
C0276651  |  aspergilloma  |  1
C0341862  |  hypothalamic amenorrhea  |  1
C1258215  |  ileus  |  1
C0162429  |  undernutrition  |  1
C0013990  |  emphysema  |  1
C0023530  |  leukopenia  |  1
C0032320  |  pneumoperitoneum  |  1
C0020598  |  hypoglycemia  |  1
C0001339  |  acute pancreatitis  |  1
C0038828  |  superior mesenteric artery syndrome  |  1
C0003469  |  anxiety disorders  |  1
C0020617  |  hypoglycemic coma  |  1
C0038353  |  gastric dilatation  |  1
C0020459  |  hyperinsulinemia  |  1
C0007222  |  cardiovascular disorders  |  1
C0031117  |  peripheral neuropathy  |  1
C1839611  |  n syndrome  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:53)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs10070190233371301007CDH9umls:C0003125BeFreeFive SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD.0.0002714422012NA526866262GA
rs100701902333713010215OLIG2umls:C0003125BeFreeFive SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD.0.0002714422012NA526866262GA
rs10070190233371302892GRIA3umls:C0003125BeFreeFive SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD.0.0002714422012NA526866262GA
rs104257124831852181AGRPumls:C0003125BeFreeAGRP rs13338499 polymorphism was associated with lowest illness-related BMI in those with AN (p = 0.0013), and NTRK2 rs1042571 was associated with highest BMI in those with BN (p = 0.0018).0.0115399742014POMC225161018GA
rs1042571248318524915NTRK2umls:C0003125BeFreeAGRP rs13338499 polymorphism was associated with lowest illness-related BMI in those with AN (p = 0.0013), and NTRK2 rs1042571 was associated with highest BMI in those with BN (p = 0.0018).0.0056342662014POMC225161018GA
rs104940672107960722854NTNG1umls:C0003125GAD[, our study suggests that both common SNPs and rare CNVs may confer genetic risk to AN.]0.0023670322011NTNG11107288236AC
rs1074815233371302892GRIA3umls:C0003125BeFreeFive SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD.0.0002714422012NANANANANA
rs10748152333713010215OLIG2umls:C0003125BeFreeFive SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD.0.0002714422012NANANANANA
rs1074815233371301007CDH9umls:C0003125BeFreeFive SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD.0.0002714422012NANANANANA
rs1117902723337130121278TPH2umls:C0003125BeFreeIn addition, rs3825885 (NTRK3, p = 9 × 10(-4)) was identified as an AN risk variant, and rs11179027 (TPH2, p = 2 × 10(-3)) as an OCD marker.0.0008143262012TPH21271983532GC
rs11179027233371304916NTRK3umls:C0003125BeFreeIn addition, rs3825885 (NTRK3, p = 9 × 10(-4)) was identified as an AN risk variant, and rs11179027 (TPH2, p = 2 × 10(-3)) as an OCD marker.0.0002714422012TPH21271983532GC
rs1176744197415689177HTR3Bumls:C0003125BeFreeIn the pilot study, we found the coding HTR3B variant, p.Y129S, (rs1176744, P = 0.004, odds ratio = 2.06) to be associated with the restrictive subtype of AN.0.0002714422009HTR3B11113932306AC
rs117837522333713010215OLIG2umls:C0003125BeFreeFive SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD.0.0002714422012NA820192013GA
rs11783752233371302892GRIA3umls:C0003125BeFreeFive SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD.0.0002714422012NA820192013GA
rs11783752233371301007CDH9umls:C0003125BeFreeFive SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD.0.0002714422012NA820192013GA
rs1333849924831852181AGRPumls:C0003125BeFreeAGRP rs13338499 polymorphism was associated with lowest illness-related BMI in those with AN (p = 0.0013), and NTRK2 rs1042571 was associated with highest BMI in those with BN (p = 0.0018).0.0115399742014LOC1019278371667486220AG
rs13338499248318524915NTRK2umls:C0003125BeFreeAGRP rs13338499 polymorphism was associated with lowest illness-related BMI in those with AN (p = 0.0013), and NTRK2 rs1042571 was associated with highest BMI in those with BN (p = 0.0018).0.0056342662014LOC1019278371667486220AG
rs147347323239044121278TPH2umls:C0003125BeFreeTPH2 (tryptophan hydroxylase 2) SNP rs1473473 was previously associated with anorexia nervosa and EDs characterized by SV.0.0008143262012TPH21272010598CT
rs204833219680270128153SPATA17umls:C0003125GAD[Identification of novel candidate loci for anorexia nervosa at 1q41 and 11q22 in Japanese by a genome-wide association analysis with microsatellite markers.]0.0023670322009LOC1053729221217936424TC
rs2295193241062422099ESR1umls:C0003125BeFreeEstrogen receptor 1 gene rs2295193 polymorphism and anorexia nervosa: new data and meta-analysis.0.0034527992013SYNE16152131959GA
rs2383378210796079472AKAP6umls:C0003125GAD[, our study suggests that both common SNPs and rare CNVs may confer genetic risk to AN.]0.0023670322011AKAP61432813264CA
rs2834070233371301007CDH9umls:C0003125BeFreeFive SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD.0.0002714422012LOC1053727842133015144GT
rs28340702333713010215OLIG2umls:C0003125BeFreeFive SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD.0.0002714422012LOC1053727842133015144GT
rs2834070233371302892GRIA3umls:C0003125BeFreeFive SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD.0.0002714422012LOC1053727842133015144GT
rs382588523337130121278TPH2umls:C0003125BeFreeIn addition, rs3825885 (NTRK3, p = 9 × 10(-4)) was identified as an AN risk variant, and rs11179027 (TPH2, p = 2 × 10(-3)) as an OCD marker.0.0008143262012NTRK31588059610TC
rs3825885233371304916NTRK3umls:C0003125BeFreeIn addition, rs3825885 (NTRK3, p = 9 × 10(-4)) was identified as an AN risk variant, and rs11179027 (TPH2, p = 2 × 10(-3)) as an OCD marker.0.0002714422012NTRK31588059610TC
rs386596687163626312693GHSRumls:C0003125BeFreeTherefore, the CC type of GHSR gene polymorphism (171T/C) is a risk factor for BN, but not for AN.0.0026384742006NANANANANA
rs38660211817435670627BDNFumls:C0003125BeFreeBrain derived neurotrophic factor gene Val66Met and -270C/T polymorphisms and personality traits predisposing to anorexia nervosa.0.1442515912007NANANANANA
rs38660211822127997627BDNFumls:C0003125BeFreeNo association of brain-derived neurotrophic factor Val66Met polymorphism with anorexia nervosa in Japanese.0.1442515912012NANANANANA
rs38660211815115760627BDNFumls:C0003125BeFreeWe previously reported a strong association of the Met66 allele of the Val66Met BDNF variant with restricting AN (ANR) and low minimum body mass index in Spanish patients.0.1442515912004NANANANANA
rs4106442107960723635SSBP2umls:C0003125GAD[, our study suggests that both common SNPs and rare CNVs may confer genetic risk to AN.]0.0023670322011NA581791715GT
rs4680146819181312COMTumls:C0003125BeFreeCombined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa.0.0120828582004COMT;MIR47612219963748GA
rs4825476233371302892GRIA3umls:C0003125BeFreeFive SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD.0.0002714422012GRIA3X123307628GA
rs48254762333713010215OLIG2umls:C0003125BeFreeFive SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD.0.0002714422012GRIA3X123307628GA
rs4825476233371301007CDH9umls:C0003125BeFreeFive SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p = 1 × 10(-3), rs4825476 (GRIA3) p = 4 × 10(-4), and rs1074815 (TPH2) p = 8 × 10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p = 2 × 10(-3) and rs11783752 (SCL18A1) p = 3 × 10(-3)), were found to be related to both AN and OCD.0.0002714422012GRIA3X123307628GA
rs503098015927146181AGRPumls:C0003125BeFreeFunctional analysis of the Ala67Thr polymorphism in agouti related protein associated with anorexia nervosa and leanness.0.0115399742005AGRP;ATP6V0D1;LOC1019278371667483042CT
rs533123210796073352HTR1Dumls:C0003125BeFreeWe confirmed that common single-nucleotide polymorphisms (SNPs) within OPRD1 (rs533123, P=0.0015) confer risk for AN, and obtained suggestive evidence that common SNPs near HTR1D (rs7532266, P=0.04) confer risk for restricting-type AN specifically.0.0059057082011OPRD1128814643GA
rs533123210796074985OPRD1umls:C0003125BeFreeWe confirmed that common single-nucleotide polymorphisms (SNPs) within OPRD1 (rs533123, P=0.0015) confer risk for AN, and obtained suggestive evidence that common SNPs near HTR1D (rs7532266, P=0.04) confer risk for restricting-type AN specifically.0.0059057082011OPRD1128814643GA
rs6590474196802704548MTRumls:C0003125BeFreeThe association analysis for MS-SNP haplotypes detected a statistically significant association (permutation P-value=0.00003) of the A-4-G-T haplotype that comprised four SNP/MS markers (rs6590474-D11S0268i-rs737582-rs7947224) on the 11q22 locus with AN.0.0002714422009CNTN51199982441AC
rs6782029210796079686VGLL4umls:C0003125GAD[, our study suggests that both common SNPs and rare CNVs may confer genetic risk to AN.]0.0023670322011VGLL4311634315TC
rs695988821079607219578ZNF804Bumls:C0003125GAD[, our study suggests that both common SNPs and rare CNVs may confer genetic risk to AN.]0.0023670322011ZNF804B788967071AG
rs6962171647290951738GHRLumls:C0003125BeFreeNo association of the Arg51Gln and Leu72Met polymorphisms of the ghrelin gene with anorexia nervosa or bulimia nervosa.0.0165316672006GHRL;GHRLOS310289773GT
rs737582196802704548MTRumls:C0003125BeFreeThe association analysis for MS-SNP haplotypes detected a statistically significant association (permutation P-value=0.00003) of the A-4-G-T haplotype that comprised four SNP/MS markers (rs6590474-D11S0268i-rs737582-rs7947224) on the 11q22 locus with AN.0.0002714422009CNTN51199992669GA
rs747302237750541815DRD4umls:C0003125BeFreeThe DRD4 C-616G and DAT1 VNTR polymorphisms correlated with several psychopathological features in patients with AN.0.004081562014DRD411636689GA,C
rs747302237750546531SLC6A3umls:C0003125BeFreeThe DRD4 C-616G and DAT1 VNTR polymorphisms correlated with several psychopathological features in patients with AN.0.0005428842014DRD411636689GA,C
rs7473022377505455885LMO3umls:C0003125BeFreeThe DRD4 C-616G and DAT1 VNTR polymorphisms correlated with several psychopathological features in patients with AN.0.0002714422014DRD411636689GA,C
rs7532266210796073352HTR1Dumls:C0003125BeFreeWe confirmed that common single-nucleotide polymorphisms (SNPs) within OPRD1 (rs533123, P=0.0015) confer risk for AN, and obtained suggestive evidence that common SNPs near HTR1D (rs7532266, P=0.04) confer risk for restricting-type AN specifically.0.0059057082011NA123225130AC
rs7532266210796074985OPRD1umls:C0003125BeFreeWe confirmed that common single-nucleotide polymorphisms (SNPs) within OPRD1 (rs533123, P=0.0015) confer risk for AN, and obtained suggestive evidence that common SNPs near HTR1D (rs7532266, P=0.04) confer risk for restricting-type AN specifically.0.0059057082011NA123225130AC
rs7947224196802704548MTRumls:C0003125BeFreeThe association analysis for MS-SNP haplotypes detected a statistically significant association (permutation P-value=0.00003) of the A-4-G-T haplotype that comprised four SNP/MS markers (rs6590474-D11S0268i-rs737582-rs7947224) on the 11q22 locus with AN.0.0002714422009CNTN511100002678TC
rs830998210796074036LRP2umls:C0003125GAD[, our study suggests that both common SNPs and rare CNVs may confer genetic risk to AN.]0.0023670322011LRP22169276576AC
rs95778821079607728215FAM155Aumls:C0003125GAD[, our study suggests that both common SNPs and rare CNVs may confer genetic risk to AN.]0.0023670322011FAM155A13107604872TC
rs983977624514567347689SOX2-OTumls:C0003125GWASCATA genome-wide association study of anorexia nervosa.0.122013SOX2-OT3181593779CT
rs99396092279736879068FTOumls:C0003125BeFreeFat mass and obesity-associated gene (FTO) in eating disorders: evidence for association of the rs9939609 obesity risk allele with bulimia nervosa and anorexia nervosa.0.0005428842012FTO1653786615TA
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:63)
CHR POS SNPID REF ALT ORI_SNPID PMID P_VALUE P_VALUE_TEXT OR/BETA CI95_TEXT GWAS_INITIAL_SAMPLE_SIZE SUB_POPULATION SUPER_POPULATION GWAS_TRAIT HPO_ID HPO_TERM DO_ID DO_TERM MESH_ID MESH_TERM EFO_ID EFO_TERM DOLITE_TERM RISK_ALLELE PUBLICATION_TYPE AA GENE_SYMBOL TYPE REFGENE
119206334rs28441017GArs28441017235684579.00E-06NA0.09[0.049-0.123] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars28441017-GTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
125469913rs2064251GArs2064251210796079.72E-06NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tG
132668428rs6425793AGrs6425793235684579.63E-06NA0.07[0.036-0.096] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars6425793-ATwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
168491995rs12069862GArs12069862235684575.42E-04NA0.11[0.046-0.174] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars12069862-GTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
179227956rs1937020CTrs1937020235684574.00E-06NA0.04[0.023-0.059] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars1937020-TTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1107830858rs10494067ACrs10494067210796076.00E-06NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC,A
1180130723rs55946907CTrs55946907235684579.00E-06NA0.07[0.037-0.095] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars55946907-CTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
274761539rs17010021TArs17010021235684571.00E-05NA0.11[0.057-0.153] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars17010021-TTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
280915114rs1370339CTrs1370339245145675.68E-05NA1.1[1.05-1.15]2,907 European ancestry cases; 14,860 European ancestry controlsEuropean(17767)ALL(17767)EUR(17767)ALL(17767)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars1370339-CResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tT
2170133086rs830998ACrs830998210796079.00E-06NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC
2223353446rs17496827ACrs17496827235684577.00E-06NA0.04[0.024-0.06] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars17496827-CTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
2225308978rs1523921TCrs1523921245145675.95E-05NA1.13[1.06-1.20]2,907 European ancestry cases; 14,860 European ancestry controlsEuropean(17767)ALL(17767)EUR(17767)ALL(17767)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars1523921-TResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC
311675789rs6782029TCrs6782029210796079.00E-06NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tT
312038264rs2618405CArs2618405245145672.03E-05NA1.15[1.08-1.23]2,907 European ancestry cases; 14,860 European ancestry controlsEuropean(17767)ALL(17767)EUR(17767)ALL(17767)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars2618405-CResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tG
3130730517rs13076493CTrs13076493235684573.34E-05NA0.04[0.023-0.063] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars13076493-CTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
3181311567rs9839776CTrs9839776245145673.00E-07NA1.16[1.10-1.23] 2,907 European ancestry cases; 14,860 European ancestry controlsEuropean(17767)ALL(17767)EUR(17767)ALL(17767)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars9839776-TResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC
45887440rs3774895ATrs3774895235684572.00E-05NA0.04[0.02-0.052] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars3774895-TTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
4102048076rs17030795AGrs17030795245145676.00E-06NA1.15[1.08-1.22] 2,907 European ancestry cases; 14,860 European ancestry controlsEuropean(17767)ALL(17767)EUR(17767)ALL(17767)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars17030795-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
4163057016rs17042030GArs17042030210796071.15E-05NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA,G
526723783rs4479806CArs4479806210796078.00E-06NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC
581074655rs457008CTrs457008210796076.96E-06NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC,T
581087534rs410644GTrs410644210796077.00E-06NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tT
594148538rs469339GArs469339235684573.00E-06NA0.14[0.083-0.205] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars469339-ATwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
5118474109rs4895185AGrs4895185235684571.69E-04NA0.03[0.015-0.051] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars4895185-ATwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
712193432rs114945094GArs114945094235684574.00E-06NA0.14[0.078-0.192] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars114945094-GTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
741295903rs11765463GArs11765463210796071.30E-05NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tG
788596385rs6959888AGrs6959888210796072.00E-06NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
7106686448rs2395833GTrs2395833245145675.62E-05NA1.1[1.05-1.15]2,907 European ancestry cases; 14,860 European ancestry controlsEuropean(17767)ALL(17767)EUR(17767)ALL(17767)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars2395833-TResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tG
7138817240rs7798474TGrs7798474235684576.90E-05NA0.04[0.019-0.059] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars7798474-TTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
7141505087rs145241704TGrs145241704235684572.00E-07NA0.14[0.09-0.196] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars145241704-TTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
7141589278rs1285957TCrs1285957235684571.00E-06NA0.06[0.032-0.08] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars1285957-CTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
7146934096rs6943628GArs6943628245145679.38E-05NA1.16[1.08-1.25]2,907 European ancestry cases; 14,860 European ancestry controlsEuropean(17767)ALL(17767)EUR(17767)ALL(17767)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars6943628-AResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tG
819540262rs11204064AGrs11204064245145671.57E-05NA1.12[1.06-1.18]2,907 European ancestry cases; 14,860 European ancestry controlsEuropean(17767)ALL(17767)EUR(17767)ALL(17767)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars11204064-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tG
886101451rs4150880TArs4150880235684571.70E-05NA0.04[0.025-0.065] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars4150880-ATwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
896504472rs77742018AGrs77742018235684574.00E-06NA0.12[0.068-0.166] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars77742018-ATwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
923874047rs512089ACrs512089210796071.98E-05NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tT
1012702569rs75263140AGrs75263140235684576.00E-06NA0.17[0.098-0.246] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars75263140-ATwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1077298609rs2043090AGrs2043090235684573.00E-06NA0.12[0.068-0.17] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars2043090-ATwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1087694292rs76765968TCrs76765968235684572.00E-06NA0.06[0.037-0.091] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars76765968-TTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1088407055rs2803546GArs2803546235684572.79E-04NA0.03[0.016-0.052] unit increase237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars2803546-GTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
10102772283rs11190790ACrs11190790235684572.02E-04NA0.03[0.014-0.05] unit increase237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars11190790-CTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
10124422108rs2421031TCrs2421031235684574.62E-04NA0.05[0.02-0.076] unit increase237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars2421031-TTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
11129910584rs3808986CArs3808986210796071.38E-05NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
1249905713rs7975712TCrs7975712210796071.68E-05NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC
1249924637rs11169058CTrs11169058210796071.44E-05NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tT
1249927148rs12296440GArs12296440210796071.24E-05NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
1249931585rs11169063TCrs11169063210796071.92E-05NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC
1250064928rs7963954AGrs7963954210796071.39E-05NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tG
1324535988rs1886797TCrs1886797245145672.18E-05NA1.13[1.07-1.20]2,907 European ancestry cases; 14,860 European ancestry controlsEuropean(17767)ALL(17767)EUR(17767)ALL(17767)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars1886797-TResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tT
1364572127rs9539891CTrs9539891245145675.88E-05NA1.12[1.06-1.19]2,907 European ancestry cases; 14,860 European ancestry controlsEuropean(17767)ALL(17767)EUR(17767)ALL(17767)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars9539891-TResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tC
1385549736rs9531686TGrs9531686235684579.00E-06NA0.04[0.022-0.054] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars9531686-TTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
13108257220rs957788TCrs957788210796078.00E-06NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
1433282470rs2383378CArs2383378210796076.00E-06NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tT
1433305020rs12894779GArs12894779210796071.54E-05NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
1580166597rs1113983CArs1113983235684571.30E-04NA0.03[0.015-0.051] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars1113983-CTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1629690904rs9933310AGrs9933310235684573.30E-05NA0.04[0.023-0.063] unit increase237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars9933310-ATwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1679186886rs8050187TCrs8050187235684577.00E-06NA0.04[0.024-0.064] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars8050187-TTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1873050334rs62090893GArs62090893235684573.00E-07NA0.09[0.052-0.118] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars62090893-GTwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
1911789015rs206863AGrs206863245145676.47E-05NA1.16[1.08-1.24]2,907 European ancestry cases; 14,860 European ancestry controlsEuropean(17767)ALL(17767)EUR(17767)ALL(17767)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars206863-GResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tA
2018079131rs17725255TCrs17725255210796072.00E-06NANANA1,033 European ancestry cases; 3,773 European ancestry pediatric controlsEuropean(4806)ALL(4806)EUR(4806)ALL(4806)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosaNAResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tT
2122335508rs10482915GArs10482915245145673.96E-05NA1.19[1.10-1.30]2,907 European ancestry cases; 14,860 European ancestry controlsEuropean(17767)ALL(17767)EUR(17767)ALL(17767)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars10482915-AResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tG
X37999652rs56156506ATrs56156506235684571.00E-06NA0.05[0.031-0.075] unit decrease237 female cases; 2,287 female controlsNOPOP(2524)ALL(2524)NOPOP(2524)ALL(2524)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars56156506-ATwin StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov't
X107692305rs5929098CTrs5929098245145678.37E-05NA1.14[1.07-1.21]2,907 European ancestry cases; 14,860 European ancestry controlsEuropean(17767)ALL(17767)EUR(17767)ALL(17767)Anorexia nervosaHPOID:0002039AnorexiaDOID:8689anorexia nervosaD000856Anorexia NervosaNANAAnorexia nervosars5929098-TResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tT
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:1)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0003125olanzapineC076029132539-06-1anorexia nervosaMESH:D000856therapeutic12616591
FDA approved drug and dosage information(Total Drugs:4)
DiseaseID Drug_name active_ingredients strength Dosage Form/Route Marketing Status TE code RLD RS
MESH:D000856zyprexaolanzapine2.5MGTABLET;ORALPrescriptionABYesNo
MESH:D000856zyprexaolanzapine10MG/VIALINJECTABLE;INTRAMUSCULARPrescriptionAPYesYes
MESH:D000856zyprexaolanzapine2.5MGTABLET;ORALPrescriptionABYesNo
MESH:D000856zyprexaolanzapine10MG/VIALINJECTABLE;INTRAMUSCULARPrescriptionAPYesYes
FDA labeling changes(Total Drugs:4)
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:D00085608/14/2008zyprexaolanzapineschizophrenia; bipolar disorderSafety and effectiveness have not been established for patients less than 18 years of age In an analysis of placebo-controlled olanzapine monotherapy studies of adolescent patients, including those with schizophrenia or bipolar disorder, olanzapine was associated with: oHyperglycemia - a statistically significantly greater mean change in fasting glucose levels compared to placebo oHyperlipidemia  statistically significant increases compared to placebo in fasting triglycerides, fasting total cholesterol and fasting LDL cholesterol oWeight gain  olanzapine treated patients gained an average of 4.6 kg, compared to an average of 0.3 kg in placebo-treated patients with a median exposure of 3 weeks; Average weight gain during long-term therapy was 7.4 kg-B---Lilly10/1/2007FALSE'
MESH:D00085608/14/2008zyprexaolanzapineschizophrenia; bipolar disorderSafety and effectiveness have not been established for patients less than 18 years of age In an analysis of placebo-controlled olanzapine monotherapy studies of adolescent patients, including those with schizophrenia or bipolar disorder, olanzapine was associated with: oHyperglycemia - a statistically significantly greater mean change in fasting glucose levels compared to placebo oHyperlipidemia  statistically significant increases compared to placebo in fasting triglycerides, fasting total cholesterol and fasting LDL cholesterol oWeight gain  olanzapine treated patients gained an average of 4.6 kg, compared to an average of 0.3 kg in placebo-treated patients with a median exposure of 3 weeks; Average weight gain during long-term therapy was 7.4 kg-B---Lilly10/1/2007FALSE'
MESH:D0008564/12/2009zyprexaolanzapineTreatment of manic or mixed episodes of bipolar I disorder and schizophrenia in adolescents ages 13-17Extended schizophrenia and manic or mixed episodes of bipolar I disorder indications from adults to adolescents 1317 years of age Safety and effectiveness in children < 13 years of age have not been established Recommended starting dose for adolescents is lower than that for adults Compared to patients from adult clinical trials, adolescents were likely to gain more weight, experience increased sedation, and have greater increases in total cholesterol, triglycerides, LDL cholesterol, prolactin and hepatic transaminase levels Information on dosing, adverse reactions, pharmacokinetics, clinical studiesLabelingB---Lilly10/1/2007TRUE'
MESH:D0008564/12/2009zyprexaolanzapineTreatment of manic or mixed episodes of bipolar I disorder and schizophrenia in adolescents ages 13-17Extended schizophrenia and manic or mixed episodes of bipolar I disorder indications from adults to adolescents 1317 years of age Safety and effectiveness in children < 13 years of age have not been established Recommended starting dose for adolescents is lower than that for adults Compared to patients from adult clinical trials, adolescents were likely to gain more weight, experience increased sedation, and have greater increases in total cholesterol, triglycerides, LDL cholesterol, prolactin and hepatic transaminase levels Information on dosing, adverse reactions, pharmacokinetics, clinical studiesLabelingB---Lilly10/1/2007TRUE'