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PedAM

Pediatric Disease Annotations & Medicines



   obstructive sleep apnea
  

Disease ID 490
Disease obstructive sleep apnea
Definition
A disorder characterized by recurrent apneas during sleep despite persistent respiratory efforts. It is due to upper airway obstruction. The respiratory pauses may induce HYPERCAPNIA or HYPOXIA. Cardiac arrhythmias and elevation of systemic and pulmonary arterial pressures may occur. Frequent partial arousals occur throughout sleep, resulting in relative SLEEP DEPRIVATION and daytime tiredness. Associated conditions include OBESITY; ACROMEGALY; MYXEDEMA; micrognathia; MYOTONIC DYSTROPHY; adenotonsilar dystrophy; and NEUROMUSCULAR DISEASES. (From Adams et al., Principles of Neurology, 6th ed, p395)
Synonym
apnea obstructive sleep
apnea obstructive sleeping
apnea, obstructive
apnea, obstructive sleep
apneas, obstructive sleep
obstructive apnea
obstructive sleep apnea (adult)(pediatric)
obstructive sleep apnea syndrome
obstructive sleep apnea syndrome (disorder)
obstructive sleep apneas
obstructive sleep apnoea
obstructive sleep apnoea (disorder)
obstructive sleep apnoea syndrome
obstructive sleep osa apnea
osa
osa - obstructive sleep apnea
osa - obstructive sleep apnoea
osahs
osas
sahs
sleep apnea (& [obstructive])
sleep apnea hypopnea syndrome
sleep apnea obstructive syndrome
sleep apnea syndrome, obstructive
sleep apnea, obstructive
sleep apnea, obstructive [disease/finding]
sleep apnea/hypopnea syndrome
sleep apneas, obstructive
sleep apnoea (& [obstructive])
sleep apnoea (& [obstructive]) (disorder)
syndrome, obstructive sleep apnea
syndrome, sleep apnea, obstructive
OMIM
DOID
UMLS
C0520679
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:159)
C0020538  |  hypertension  |  33
C0948265  |  metabolic syndrome  |  25
C0028754  |  obesity  |  24
C0042373  |  vascular disease  |  23
C0007222  |  cardiovascular disease  |  20
C0011847  |  diabetes  |  15
C0011860  |  type 2 diabetes  |  14
C0042373  |  vascular diseases  |  11
C0010068  |  coronary artery disease  |  10
C0011570  |  depression  |  10
C0007222  |  cardiovascular diseases  |  9
C0242350  |  erectile dysfunction  |  7
C0017168  |  oesophageal reflux  |  7
C0017168  |  gastroesophageal reflux  |  7
C0017168  |  esophageal reflux  |  7
C0004153  |  atherosclerosis  |  6
C0024117  |  chronic obstructive pulmonary disease  |  6
C0037317  |  sleep disturbance  |  6
C0017601  |  glaucoma  |  5
C0271650  |  glucose intolerance  |  5
C0027051  |  myocardial infarction  |  5
C0027051  |  myocardial infarct  |  5
C0003467  |  anxiety  |  5
C0030567  |  parkinson's disease  |  5
C0600260  |  obstructive pulmonary disease  |  5
C0024115  |  lung disease  |  4
C0011849  |  diabetes mellitus  |  4
C0018799  |  heart disease  |  4
C0034065  |  pulmonary embolism  |  4
C0028756  |  severe obesity  |  4
C0026769  |  multiple sclerosis  |  4
C0023895  |  liver disease  |  4
C0024115  |  pulmonary disease  |  4
C0024117  |  chronic obstructive pulmonary disease (copd)  |  4
C0004096  |  asthma  |  4
C0011860  |  type 2 diabetes mellitus  |  3
C0010278  |  craniosynostosis  |  3
C0679466  |  cognitive deficits  |  3
C0027404  |  narcolepsy  |  3
C1800706  |  idiopathic pulmonary fibrosis  |  3
C0037315  |  sleep apnea  |  3
C0018801  |  heart failure  |  3
C0851578  |  sleep disorders  |  3
C0017168  |  gastroesophageal reflux disease  |  3
C0037317  |  sleep disturbances  |  3
C0017168  |  esophageal reflux disease  |  3
C0751774  |  periodic limb movement  |  3
C2607914  |  allergic rhinitis  |  3
C0159069  |  impaired glucose tolerance  |  3
C0020542  |  pulmonary hypertension  |  3
C0034069  |  pulmonary fibrosis  |  3
C0155626  |  acute myocardial infarction  |  3
C0032460  |  polycystic ovary syndrome  |  2
C0035328  |  retinal vein occlusion  |  2
C0151740  |  intracranial hypertension  |  2
C1535927  |  charge syndrome  |  2
C0042373  |  vascular disorder  |  2
C0032461  |  polycythemia  |  2
C0033953  |  sexual dysfunction  |  2
C0042373  |  vascular disorders  |  2
C0520680  |  central sleep apnea  |  2
C0008924  |  cleft lip  |  2
C0022661  |  end-stage renal disease  |  2
C0007222  |  cardiovascular disorders  |  2
C0442874  |  neuropathy  |  2
C0751772  |  rem sleep behavior disorder  |  2
C0751711  |  anterior ischemic optic neuropathy  |  2
C0014544  |  epilepsy  |  2
C0022578  |  keratoconus  |  2
C0206062  |  interstitial lung disease  |  2
C0035078  |  renal failure  |  2
C0008925  |  cleft palate  |  2
C0022116  |  ischemia  |  2
C0001206  |  acromegaly  |  2
C0024115  |  lung diseases  |  2
C2697932  |  loeys-dietz syndrome  |  1
C0029132  |  optic neuropathy  |  1
C0026948  |  mycosis fungoides  |  1
C0011269  |  vascular dementia  |  1
C0006325  |  bruxism  |  1
C0020538  |  systemic hypertension  |  1
C0023976  |  long qt syndrome  |  1
C0032914  |  preeclampsia  |  1
C0041696  |  major depressive disorder  |  1
C0016522  |  patent foramen ovale  |  1
C0005586  |  bipolar disorder  |  1
C1956089  |  osteophytes  |  1
C0030567  |  parkinson disease  |  1
C0026896  |  myasthenia gravis  |  1
C0271084  |  exudative age-related macular degeneration  |  1
C0032460  |  polycystic ovary  |  1
C0751774  |  periodic limb movement disorder  |  1
C0010273  |  crouzon syndrome  |  1
C0004763  |  barrett's esophagus  |  1
C0002895  |  sickle cell anemia  |  1
C0033845  |  idiopathic intracranial hypertension  |  1
C0027051  |  myocardial infarction (mi)  |  1
C0020498  |  forestier disease  |  1
C0949690  |  spondyloarthritis  |  1
C1318533  |  secondary polycythemia  |  1
C0028756  |  morbid obesity  |  1
C0042075  |  urological diseases  |  1
C0013080  |  trisomy 21  |  1
C0149931  |  migraine  |  1
C0007273  |  carotid artery disease  |  1
C0004779  |  gorlin syndrome  |  1
C0853193  |  bipolar i disorder  |  1
C0026266  |  mitral regurgitation  |  1
C0003874  |  septic arthritis  |  1
C0025235  |  melkersson-rosenthal syndrome  |  1
C0001627  |  congenital adrenal hyperplasia  |  1
C0033375  |  prolactinoma  |  1
C0007194  |  hypertrophic cardiomyopathy  |  1
C0003872  |  psoriatic arthritis  |  1
C0022661  |  end-stage renal failure  |  1
C1621895  |  adrenal hyperplasia  |  1
C0026850  |  muscular dystrophy  |  1
C0152136  |  normal tension glaucoma  |  1
C0010278  |  craniosynostosis syndromes  |  1
C0238288  |  facioscapulohumeral muscular dystrophy  |  1
C0024437  |  age-related macular degeneration  |  1
C0003486  |  aortic aneurysms  |  1
C0162871  |  abdominal aortic aneurysm  |  1
C0018799  |  heart diseases  |  1
C0020676  |  hypothyroidism  |  1
C0032285  |  pneumonia  |  1
C0600260  |  obstructive lung diseases  |  1
C0028754  |  adiposity  |  1
C0038013  |  ankylosing spondylitis  |  1
C0154841  |  central retinal vein occlusion  |  1
C0024437  |  macular degeneration  |  1
C0018916  |  hemangioma  |  1
C0009241  |  cognitive disorders  |  1
C0003493  |  aortic disease  |  1
C0151744  |  myocardial ischemia  |  1
C0030286  |  pancreatic disease  |  1
C0027765  |  neurological disease  |  1
C0206062  |  interstitial lung diseases  |  1
C0600260  |  obstructive lung disease  |  1
C0000889  |  acanthosis nigricans  |  1
C0040128  |  thyroid disease  |  1
C0029882  |  otitis media  |  1
C0162871  |  abdominal aortic aneurysms  |  1
C0033975  |  psychosis  |  1
C0026703  |  mucopolysaccharidoses  |  1
C0005586  |  bipolar affective disorder  |  1
C0020538  |  increased blood pressure  |  1
C0035455  |  rhinitis  |  1
C0024796  |  marfan's syndrome  |  1
C0010068  |  coronary heart disease  |  1
C0022658  |  renal disease  |  1
C0878544  |  cardiomyopathy  |  1
C0003864  |  arthritis  |  1
C0033687  |  proteinuria  |  1
C0030319  |  panic disorder  |  1
C0026703  |  mucopolysaccharidosis  |  1
C0151740  |  increased intracranial pressure  |  1
C0025281  |  meniere's disease  |  1
C0003486  |  aortic aneurysm  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
EDNRA  |  1909  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:57)
348  |  APOE  |  infer
1636  |  ACE  |  infer
5054  |  SERPINE1  |  infer
147  |  ADRA1B  |  infer
150  |  ADRA2A  |  infer
153  |  ADRB1  |  infer
154  |  ADRB2  |  infer
429  |  ASCL1  |  infer
627  |  BDNF  |  infer
886  |  CCKAR  |  infer
1401  |  CRP  |  infer
1535  |  CYBA  |  infer
1889  |  ECE1  |  infer
1906  |  EDN1  |  infer
1908  |  EDN3  |  infer
1909  |  EDNRA  |  infer
2260  |  FGFR1  |  infer
2263  |  FGFR2  |  infer
2261  |  FGFR3  |  infer
2550  |  GABBR1  |  infer
2668  |  GDNF  |  infer
2678  |  GGT1  |  infer
2784  |  GNB3  |  infer
3062  |  HCRTR2  |  infer
3091  |  HIF1A  |  infer
3351  |  HTR1B  |  infer
3356  |  HTR2A  |  infer
3358  |  HTR2C  |  infer
3359  |  HTR3A  |  infer
9177  |  HTR3B  |  infer
170572  |  HTR3C  |  infer
200909  |  HTR3D  |  infer
285242  |  HTR3E  |  infer
3553  |  IL1B  |  infer
3569  |  IL6  |  infer
51141  |  INSIG2  |  infer
3667  |  IRS1  |  infer
3952  |  LEP  |  infer
3953  |  LEPR  |  infer
4023  |  LPL  |  infer
4159  |  MC3R  |  infer
4160  |  MC4R  |  infer
4487  |  MSX1  |  infer
4488  |  MSX2  |  infer
4524  |  MTHFR  |  infer
4692  |  NDN  |  infer
4846  |  NOS3  |  infer
8929  |  PHOX2B  |  infer
5376  |  PMP22  |  infer
5979  |  RET  |  infer
6469  |  SHH  |  infer
6532  |  SLC6A4  |  infer
6949  |  TCOF1  |  infer
7046  |  TGFBR1  |  infer
7124  |  TNF  |  infer
7351  |  UCP2  |  infer
7352  |  UCP3  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:275)
6376  |  CX3CL1  |  DISEASES
54814  |  QPCTL  |  DISEASES
6583  |  SLC22A4  |  DISEASES
28954  |  REM1  |  DISEASES
6634  |  SNRPD3  |  DISEASES
3162  |  HMOX1  |  DISEASES
328  |  APEX1  |  DISEASES
7076  |  TIMP1  |  DISEASES
479  |  ATP12A  |  DISEASES
4313  |  MMP2  |  DISEASES
1666  |  DECR1  |  DISEASES
56729  |  RETN  |  DISEASES
5444  |  PON1  |  DISEASES
5054  |  SERPINE1  |  DISEASES
8985  |  PLOD3  |  DISEASES
6347  |  CCL2  |  DISEASES
4621  |  MYH3  |  DISEASES
952  |  CD38  |  DISEASES
8929  |  PHOX2B  |  DISEASES
6783  |  SULT1E1  |  DISEASES
4048  |  LTA4H  |  DISEASES
3565  |  IL4  |  DISEASES
56920  |  SEMA3G  |  DISEASES
4057  |  LTF  |  DISEASES
338  |  APOB  |  DISEASES
6402  |  SELL  |  DISEASES
335  |  APOA1  |  DISEASES
9525  |  VPS4B  |  DISEASES
4852  |  NPY  |  DISEASES
3759  |  KCNJ2  |  DISEASES
11017  |  SNRNP27  |  DISEASES
2806  |  GOT2  |  DISEASES
2354  |  FOSB  |  DISEASES
51119  |  SBDS  |  DISEASES
3630  |  INS  |  DISEASES
3741  |  KCNA5  |  DISEASES
348  |  APOE  |  DISEASES
4142  |  MAS1  |  DISEASES
2056  |  EPO  |  DISEASES
9104  |  RGN  |  DISEASES
1401  |  CRP  |  DISEASES
1131  |  CHRM3  |  DISEASES
4622  |  MYH4  |  DISEASES
1116  |  CHI3L1  |  DISEASES
284904  |  SEC14L4  |  DISEASES
2167  |  FABP4  |  DISEASES
759  |  CA1  |  DISEASES
3569  |  IL6  |  DISEASES
5004  |  ORM1  |  DISEASES
1419  |  CRYGB  |  DISEASES
1535  |  CYBA  |  DISEASES
64398  |  MPP5  |  DISEASES
6532  |  SLC6A4  |  DISEASES
4223  |  MEOX2  |  DISEASES
23531  |  MMD  |  DISEASES
9480  |  ONECUT2  |  DISEASES
6521  |  SLC4A1  |  DISEASES
495  |  ATP4A  |  DISEASES
11316  |  COPE  |  DISEASES
25939  |  SAMHD1  |  DISEASES
84954  |  MPND  |  DISEASES
57084  |  SLC17A6  |  DISEASES
2033  |  EP300  |  DISEASES
50507  |  NOX4  |  DISEASES
3553  |  IL1B  |  DISEASES
54414  |  SIAE  |  DISEASES
6403  |  SELP  |  DISEASES
4162  |  MCAM  |  DISEASES
5443  |  POMC  |  DISEASES
8626  |  TP63  |  DISEASES
3383  |  ICAM1  |  DISEASES
3827  |  KNG1  |  DISEASES
10058  |  ABCB6  |  DISEASES
22937  |  SCAP  |  DISEASES
54806  |  AHI1  |  DISEASES
161253  |  REM2  |  DISEASES
5678  |  PSG9  |  DISEASES
93650  |  ACPT  |  DISEASES
402665  |  IGLON5  |  DISEASES
5972  |  REN  |  DISEASES
3484  |  IGFBP1  |  DISEASES
3934  |  LCN2  |  DISEASES
4851  |  NOTCH1  |  DISEASES
133  |  ADM  |  DISEASES
3606  |  IL18  |  DISEASES
57105  |  CYSLTR2  |  DISEASES
9320  |  TRIP12  |  DISEASES
22808  |  MRAS  |  DISEASES
653361  |  NCF1  |  DISEASES
10481  |  HOXB13  |  DISEASES
1636  |  ACE  |  DISEASES
5152  |  PDE9A  |  DISEASES
6285  |  S100B  |  DISEASES
9442  |  MED27  |  DISEASES
5675  |  PSG6  |  DISEASES
10898  |  CPSF4  |  DISEASES
3060  |  HCRT  |  DISEASES
7412  |  VCAM1  |  DISEASES
213  |  ALB  |  DISEASES
51304  |  ZDHHC3  |  DISEASES
6059  |  ABCE1  |  DISEASES
81789  |  TIGD6  |  DISEASES
25862  |  USP49  |  DISEASES
4846  |  NOS3  |  DISEASES
5267  |  SERPINA4  |  DISEASES
219793  |  TBATA  |  DISEASES
6236  |  RRAD  |  DISEASES
4640  |  MYO1A  |  DISEASES
2819  |  GPD1  |  DISEASES
7001  |  PRDX2  |  DISEASES
80150  |  ASRGL1  |  DISEASES
4054  |  LTBP3  |  DISEASES
116844  |  LRG1  |  DISEASES
3479  |  IGF1  |  DISEASES
2357  |  FPR1  |  DISEASES
8862  |  APLN  |  DISEASES
2548  |  GAA  |  DISEASES
81851  |  KRTAP1-1  |  DISEASES
2353  |  FOS  |  DISEASES
27289  |  RND1  |  DISEASES
51316  |  PLAC8  |  DISEASES
169270  |  ZNF596  |  DISEASES
836  |  CASP3  |  DISEASES
91464  |  ISX  |  DISEASES
133522  |  PPARGC1B  |  DISEASES
3952  |  LEP  |  DISEASES
5062  |  PAK2  |  DISEASES
1909  |  EDNRA  |  DISEASES
53905  |  DUOX1  |  DISEASES
5680  |  PSG11  |  DISEASES
8289  |  ARID1A  |  DISEASES
9322  |  TRIP10  |  DISEASES
9370  |  ADIPOQ  |  DISEASES
220032  |  GDPD4  |  DISEASES
6517  |  SLC2A4  |  DISEASES
6863  |  TAC1  |  DISEASES
9242  |  MSC  |  DISEASES
10743  |  RAI1  |  DISEASES
7586  |  ZKSCAN1  |  DISEASES
199699  |  DAND5  |  DISEASES
5032  |  P2RY11  |  DISEASES
2200  |  FBN1  |  DISEASES
3052  |  HCCS  |  DISEASES
64327  |  LMBR1  |  DISEASES
5034  |  P4HB  |  DISEASES
255324  |  EPGN  |  DISEASES
3953  |  LEPR  |  DISEASES
277  |  AMY1B  |  DISEASES
6401  |  SELE  |  DISEASES
29940  |  DSE  |  DISEASES
5671  |  PSG3  |  DISEASES
23768  |  FLRT2  |  DISEASES
10732  |  TCFL5  |  DISEASES
51738  |  GHRL  |  DISEASES
3988  |  LIPA  |  DISEASES
3363  |  HTR7  |  DISEASES
3091  |  HIF1A  |  DISEASES
51337  |  THEM6  |  DISEASES
222236  |  NAPEPLD  |  DISEASES
3770  |  KCNJ14  |  DISEASES
7137  |  TNNI3  |  DISEASES
145264  |  SERPINA12  |  DISEASES
344901  |  OSTN  |  DISEASES
6633  |  SNRPD2  |  DISEASES
60490  |  PPCDC  |  DISEASES
5348  |  FXYD1  |  DISEASES
5673  |  PSG5  |  DISEASES
57492  |  ARID1B  |  DISEASES
3921  |  RPSA  |  DISEASES
2879  |  GPX4  |  DISEASES
50618  |  ITSN2  |  DISEASES
3359  |  HTR3A  |  DISEASES
6720  |  SREBF1  |  DISEASES
6651  |  SON  |  DISEASES
6714  |  SRC  |  DISEASES
26057  |  ANKRD17  |  DISEASES
56980  |  PRDM10  |  DISEASES
11086  |  ADAM29  |  DISEASES
6241  |  RRM2  |  DISEASES
1565  |  CYP2D6  |  DISEASES
5167  |  ENPP1  |  DISEASES
8532  |  CPZ  |  DISEASES
6721  |  SREBF2  |  DISEASES
4215  |  MAP3K3  |  DISEASES
56259  |  CTNNBL1  |  DISEASES
9937  |  DCLRE1A  |  DISEASES
22796  |  COG2  |  DISEASES
7139  |  TNNT2  |  DISEASES
2117  |  ETV3  |  DISEASES
8991  |  SELENBP1  |  DISEASES
4170  |  MCL1  |  DISEASES
8266  |  UBL4A  |  DISEASES
9446  |  GSTO1  |  DISEASES
50861  |  STMN3  |  DISEASES
278  |  AMY1C  |  DISEASES
276  |  AMY1A  |  DISEASES
6319  |  SCD  |  DISEASES
959  |  CD40LG  |  DISEASES
9532  |  BAG2  |  DISEASES
5730  |  PTGDS  |  DISEASES
154796  |  AMOT  |  DISEASES
7422  |  VEGFA  |  DISEASES
6441  |  SFTPD  |  DISEASES
4318  |  MMP9  |  DISEASES
79717  |  PPCS  |  DISEASES
1979  |  EIF4EBP2  |  DISEASES
10800  |  CYSLTR1  |  DISEASES
2170  |  FABP3  |  DISEASES
7295  |  TXN  |  DISEASES
1896  |  EDA  |  DISEASES
4686  |  NCBP1  |  DISEASES
3055  |  HCK  |  DISEASES
4879  |  NPPB  |  DISEASES
4878  |  NPPA  |  DISEASES
1471  |  CST3  |  DISEASES
10159  |  ATP6AP2  |  DISEASES
1536  |  CYBB  |  DISEASES
3356  |  HTR2A  |  DISEASES
5251  |  PHEX  |  DISEASES
1906  |  EDN1  |  DISEASES
25820  |  ARIH1  |  DISEASES
390598  |  SKOR1  |  DISEASES
551  |  AVP  |  DISEASES
6462  |  SHBG  |  DISEASES
241  |  ALOX5AP  |  DISEASES
3486  |  IGFBP3  |  DISEASES
9189  |  ZBED1  |  DISEASES
11082  |  ESM1  |  DISEASES
55835  |  CENPJ  |  DISEASES
26278  |  SACS  |  DISEASES
81623  |  DEFB126  |  DISEASES
6545  |  SLC7A4  |  DISEASES
1133  |  CHRM5  |  DISEASES
9467  |  SH3BP5  |  DISEASES
56953  |  NT5M  |  DISEASES
50506  |  DUOX2  |  DISEASES
83696  |  TRAPPC9  |  DISEASES
11262  |  SP140  |  DISEASES
3703  |  STT3A  |  DISEASES
55188  |  RIC8B  |  DISEASES
23041  |  MON2  |  DISEASES
51520  |  LARS  |  DISEASES
64115  |  C10orf54  |  DISEASES
84709  |  MGARP  |  DISEASES
375704  |  ENHO  |  DISEASES
56903  |  PAPOLB  |  DISEASES
5672  |  PSG4  |  DISEASES
5670  |  PSG2  |  DISEASES
114781  |  BTBD9  |  DISEASES
55660  |  PRPF40A  |  DISEASES
1123  |  CHN1  |  DISEASES
199800  |  ADM5  |  DISEASES
197  |  AHSG  |  DISEASES
6503  |  SLA  |  DISEASES
23705  |  CADM1  |  DISEASES
3550  |  IK  |  DISEASES
7124  |  TNF  |  DISEASES
4152  |  MBD1  |  DISEASES
54900  |  LAX1  |  DISEASES
1132  |  CHRM4  |  DISEASES
2263  |  FGFR2  |  DISEASES
3586  |  IL10  |  DISEASES
627  |  BDNF  |  DISEASES
2638  |  GC  |  DISEASES
100506742  |  CASP12  |  DISEASES
57451  |  TENM2  |  DISEASES
3347  |  HTN3  |  DISEASES
83695  |  RHNO1  |  DISEASES
1649  |  DDIT3  |  DISEASES
101  |  ADAM8  |  DISEASES
389422  |  C6orf183  |  DISEASES
7138  |  TNNT1  |  DISEASES
79990  |  PLEKHH3  |  DISEASES
102191832  |  FBXW7-AS1  |  DISEASES
26807  |  SNORD43  |  DISEASES
Locus(Waiting for update.)
Disease ID 490
Disease obstructive sleep apnea
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:4)
HP:0000458  |  Anosmia
HP:0001262  |  Somnolence
HP:0002870  |  Obstructive sleep apnea
HP:0002384  |  Dyscognitive seizures
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:142)
HP:0001262  |  Somnolence  |  42
HP:0000822  |  Hypertension  |  33
HP:0001513  |  Obesity  |  20
HP:0100543  |  Cognitive deficits  |  16
HP:0002104  |  Absence of spontaneous respiration  |  15
HP:0001297  |  Cerebral vascular events  |  13
HP:0040213  |  Hypopnea  |  12
HP:0100786  |  Excessive sleepiness  |  11
HP:0000716  |  Depression  |  10
HP:0005110  |  Atrial fibrillation  |  10
HP:0001677  |  Coronary artery disease  |  10
HP:0100785  |  Insomnia  |  10
HP:0002189  |  Excessive daytime sleepiness  |  10
HP:0002020  |  Heartburn  |  9
HP:0012418  |  Low blood oxygen level  |  9
HP:0000833  |  Glucose intolerance  |  8
HP:0000855  |  Insulin resistance  |  7
HP:0012378  |  Fatigue  |  7
HP:0000802  |  Erectile dysfunction  |  7
HP:0002140  |  Ischemic stroke  |  7
HP:0006510  |  Chronic obstructive pulmonary disease  |  6
HP:0002621  |  Atherosclerosis  |  6
HP:0011675  |  Arrhythmias  |  6
HP:0002360  |  Sleep disturbance  |  6
HP:0000739  |  Anxiety  |  5
HP:0001742  |  Obstruction of nose  |  5
HP:0002781  |  Upper airway obstruction  |  5
HP:0030812  |  Tonsillar hypertrophy  |  5
HP:0001658  |  Myocardial infarction  |  5
HP:0000501  |  Glaucoma  |  5
HP:0002099  |  Asthma  |  4
HP:0000819  |  Diabetes mellitus  |  4
HP:0001397  |  Hepatic steatosis  |  4
HP:0002871  |  Central apnea  |  4
HP:0000805  |  Enuresis  |  4
HP:0001824  |  Weight loss  |  4
HP:0012416  |  Hypercarbia  |  4
HP:0002204  |  Pulmonary embolism  |  3
HP:0002206  |  Pulmonary fibrosis  |  3
HP:0012384  |  Nasal inflammation  |  3
HP:0001363  |  Early fusion of cranial sutures  |  3
HP:0030050  |  Narcolepsy  |  3
HP:0002092  |  Pulmonary artery hypertension  |  3
HP:0001635  |  Congestive heart failure  |  3
HP:0002315  |  Headaches  |  3
HP:0010535  |  Sleep apnea  |  3
HP:0003193  |  Allergic rhinitis  |  3
HP:0003774  |  End-stage renal failure  |  3
HP:0000175  |  Palatoschisis  |  2
HP:0010677  |  Enuresis nocturna  |  2
HP:0007634  |  Nonarteritic anterior ischemic optic neuropathy  |  2
HP:0000201  |  Pierre-robin deformity  |  2
HP:0001694  |  Right-to-left shunt  |  2
HP:0000563  |  Conical cornea  |  2
HP:0000845  |  Acromegalic growth  |  2
HP:0012743  |  Central obesity  |  2
HP:0002459  |  Dysautonomia  |  2
HP:0000752  |  Hyperactive behavior  |  2
HP:0001250  |  Seizures  |  2
HP:0000083  |  Renal insufficiency  |  2
HP:0006530  |  Interstitial lung disease  |  2
HP:0001601  |  Laryngomalacia  |  2
HP:0001901  |  Abnormally shaped erythrocytes  |  2
HP:0002516  |  Intracranial pressure elevation  |  2
HP:0002791  |  Under breathing  |  2
HP:0011800  |  Midface, flat  |  2
HP:0000017  |  Nocturia  |  2
HP:0002329  |  Drowsiness  |  2
HP:0012636  |  Retinal vein occlusion  |  2
HP:0001653  |  Mitral valve insufficiency  |  1
HP:0012594  |  High urine albumin levels  |  1
HP:0000956  |  Keratosis nigricans  |  1
HP:0012228  |  Tension-type headache  |  1
HP:0002180  |  Neurodegeneration  |  1
HP:0002090  |  Pneumonia  |  1
HP:0012531  |  Pain  |  1
HP:0003394  |  Muscle cramps  |  1
HP:0005943  |  Respiratory arrest  |  1
HP:0008221  |  Enlarged adrenal glands  |  1
HP:0001028  |  Strawberry mark  |  1
HP:0000303  |  Increased size of lower jaw  |  1
HP:0010518  |  Thyroglossal cyst  |  1
HP:0100602  |  Pre-eclampsia  |  1
HP:0002635  |  Atheromatosis  |  1
HP:0001369  |  Arthritis  |  1
HP:0000608  |  Macular degeneration  |  1
HP:0008258  |  Congenital adrenal hyperplasia  |  1
HP:0001717  |  Coronary artery calcification  |  1
HP:0002597  |  Abnormality of blood vessels  |  1
HP:0001138  |  Damaged optic nerve  |  1
HP:0100580  |  Barrett's esophagus  |  1
HP:0000820  |  Thyroid abnormality  |  1
HP:0008970  |  Scapulohumeral muscular dystrophy  |  1
HP:0003095  |  Septic arthritis  |  1
HP:0005321  |  Mandibulofacial dysostosis  |  1
HP:0000158  |  Abnormally large tongue  |  1
HP:0001907  |  Thromboembolic disease  |  1
HP:0000093  |  Proteinuria  |  1
HP:0002015  |  Swallowing difficulty  |  1
HP:0005957  |  Abnormal breathing  |  1
HP:0000969  |  Dropsy  |  1
HP:0012196  |  Periodic respiration  |  1
HP:0001655  |  Patent foramen ovale  |  1
HP:0001605  |  Vocal cord paralysis  |  1
HP:0007302  |  Bipolar disorder  |  1
HP:0001288  |  Gait disturbance  |  1
HP:0001342  |  Intracerebral hemorrhage  |  1
HP:0000924  |  Abnormality of the skeletal system  |  1
HP:0001657  |  Prolonged QT interval  |  1
HP:0001510  |  Growth deficiency  |  1
HP:0002094  |  Dyspnea  |  1
HP:0001649  |  Tachycardia  |  1
HP:0012820  |  Bilateral vocal cord paralysis  |  1
HP:0006536  |  Obstructive lung disease  |  1
HP:0002076  |  Migraine headaches  |  1
HP:0000709  |  Psychosis  |  1
HP:0004953  |  Abdominal aortic aneurysm  |  1
HP:0000388  |  Otitis media  |  1
HP:0001638  |  Cardiomyopathy  |  1
HP:0000327  |  Maxillary micrognathia  |  1
HP:0004439  |  Crouzon syndrome  |  1
HP:0007868  |  ARMD  |  1
HP:0010536  |  Central sleep apnoea  |  1
HP:0003560  |  Muscular dystrophy  |  1
HP:0009118  |  Hypoplasia of lower jaw  |  1
HP:0012592  |  Albuminuria  |  1
HP:0002617  |  Aneurysmal dilatation  |  1
HP:0100022  |  Movement disorder  |  1
HP:0003473  |  Fatigable weakness  |  1
HP:0000347  |  Hypoplasia of mandible  |  1
HP:0001639  |  Hypertrophic cardiomyopathy  |  1
HP:0002354  |  Memory loss  |  1
HP:0200136  |  Oral-pharyngeal dysphagia  |  1
HP:0001645  |  Sudden cardiac death  |  1
HP:0004749  |  Atrial flutter  |  1
HP:0000147  |  Sclerocystic ovaries  |  1
HP:0000713  |  Agitation  |  1
HP:0000821  |  Underactive thyroid  |  1
HP:0000689  |  Misalignment of upper and lower dental arches  |  1
HP:0100827  |  Lymphocytosis  |  1
HP:0003763  |  Bruxism  |  1
HP:0004942  |  Aortic aneurysm  |  1
Disease ID 490
Disease obstructive sleep apnea
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:43)
C0020538  |  hypertension  |  32
C0948265  |  metabolic syndrome  |  24
C0028754  |  obesity  |  20
C0042373  |  vascular disease  |  17
C0007222  |  cardiovascular disease  |  15
C0011860  |  type 2 diabetes  |  14
C1301700  |  cardiovascular morbidity  |  13
C0038454  |  stroke  |  13
C0427008  |  stiffness  |  11
C0917799  |  excessive sleepiness  |  11
C0856169  |  endothelial dysfunction  |  11
C0011570  |  depression  |  10
C0694563  |  excessive daytime sleepiness  |  10
C0001883  |  airway obstruction  |  9
C0015672  |  fatigue  |  7
C0037384  |  snoring  |  7
C0004153  |  atherosclerosis  |  6
C0017168  |  gastroesophageal reflux  |  6
C0042373  |  vascular diseases  |  6
C0740852  |  upper airway obstruction  |  5
C0027051  |  myocardial infarction  |  5
C1393529  |  vascular complications  |  5
C0007222  |  cardiovascular diseases  |  5
C0520680  |  central apnea  |  4
C0024115  |  pulmonary disease  |  4
C0020440  |  hypercapnia  |  4
C0851578  |  sleep disorders  |  3
C0155626  |  acute myocardial infarction  |  3
C0020542  |  pulmonary hypertension  |  3
C0028734  |  nocturia  |  2
C0017168  |  gastroesophageal reflux disease  |  2
C0086132  |  depressive symptoms  |  2
C0031880  |  obesity hypoventilation syndrome  |  1
C0694563  |  excessive daytime somnolence  |  1
C0020440  |  carbon dioxide retention  |  1
C0079035  |  bradyarrhythmia  |  1
C0339084  |  floppy eyelid syndrome  |  1
C0010068  |  coronary heart disease  |  1
C0878544  |  cardiomyopathy  |  1
C0033687  |  proteinuria  |  1
C0021888  |  intraocular pressure  |  1
C0026635  |  mouth breathing  |  1
C0422833  |  ent symptoms  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:20)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs10433310224513323630INSumls:C0520679BeFreeChildhood OSA is associated with higher plasma MIF, hsCRP, and fasting insulin levels that promote cardiometabolic risk, and the MIF gene SNP rs10433310 may account for some of the variance in such risk.0.0005428842012MIF-AS12223896636GA
rs11126184231554141902LPAR1umls:C0520679BeFreeUsing a panel of 46,449 polymorphisms from roughly 2,100 candidate genes on a customized Illumina iSelect chip, we tested for association with the apnea hypopnea index (AHI) as well as moderate to severe OSA (AHI≥15) in 3,551 participants of the Cleveland Family Study and two cohorts participating in the Sleep Heart Health Study.Among 647 African-Americans, rs11126184 in the pleckstrin (PLEK) gene was associated with OSA while rs7030789 in the lysophosphatidic acid receptor 1 (LPAR1) gene was associated with AHI using a chip-wide significance threshold of p-value<2×10(-6).0.0002714422012NA268425042CA
rs11126184231554145341PLEKumls:C0520679BeFreeUsing a panel of 46,449 polymorphisms from roughly 2,100 candidate genes on a customized Illumina iSelect chip, we tested for association with the apnea hypopnea index (AHI) as well as moderate to severe OSA (AHI≥15) in 3,551 participants of the Cleveland Family Study and two cohorts participating in the Sleep Heart Health Study.Among 647 African-Americans, rs11126184 in the pleckstrin (PLEK) gene was associated with OSA while rs7030789 in the lysophosphatidic acid receptor 1 (LPAR1) gene was associated with AHI using a chip-wide significance threshold of p-value<2×10(-6).0.0002714422012NA268425042CA
rs13170573254741156444SGCDumls:C0520679BeFreeThe CC genotype of the delta-sarcoglycan gene polymorphism rs13170573 is associated with obstructive sleep apnea in the Chinese population.0.0002714422014SGCD;LOC1053776745156327182CG
rs1409986231554145733PTGER3umls:C0520679BeFreeAmong 2,904 individuals of European ancestry, rs1409986 in the prostaglandin E2 receptor (PTGER3) gene was significantly associated with OSA.0.0002714422012PTGER3170865815AG
rs1800629220431167124TNFumls:C0520679BeFreeOnly TNFA rs1800629 was significantly associated with OSA under an allele frequency model (3 studies, odds ratio [OR] = 1.82, 95% confidence interval [CI] 1.26-2.61).0.0154497812011TNF631575254GA
rs386602276162582053358HTR2Cumls:C0520679BeFreeGenotypes and allele frequencies of 102T/C polymorphism of the HTR2A and 796G/C polymorphism of the HTR2C did not differ between controls and patients with OSA.0.0050055062005NANANANANA
rs386602276240655383356HTR2Aumls:C0520679BeFreeAssociation between the -1438G/A and T102C polymorphisms of 5-HT2A receptor gene and obstructive sleep apnea: a meta-analysis.0.0071770412013NANANANANA
rs386602276162582053356HTR2Aumls:C0520679BeFreeGenotypes and allele frequencies of 102T/C polymorphism of the HTR2A and 796G/C polymorphism of the HTR2C did not differ between controls and patients with OSA.0.0071770412005NANANANANA
rs4673219025981535CYBAumls:C0520679BeFreeThe frequencies of NADPH oxidase (NOX) polymorphisms in the p22phox subunit were similar between children with OSA and controls, except for rs6520785 and rs4673, the latter being significantly more frequent among the OSA children without deficits than with deficits (p<0.02).0.0031813582012CYBA1688646828AG
rs475144020405330594857NPSumls:C0520679BeFreeWe investigated the association of the non-synonymous polymorphism rs4751440 in the NPS precursor gene with OSAS and certain variables related to OSAS (daytime sleepiness, body mass index (BMI), insulin resistance, and blood pressure).0.0002714422011NPS10127552592GA,C
rs5370185800621906EDN1umls:C0520679BeFreeEndothelin-1 gene variant Lys198Asn and plasma endothelin level in obstructive sleep apnea.0.0906397722009EDN1612296022GT
rs6313162582053356HTR2Aumls:C0520679BeFreeGenotypes and allele frequencies of 102T/C polymorphism of the HTR2A and 796G/C polymorphism of the HTR2C did not differ between controls and patients with OSA.0.0071770412005HTR2A1346895805GA
rs6313240655383356HTR2Aumls:C0520679BeFreeAssociation between the -1438G/A and T102C polymorphisms of 5-HT2A receptor gene and obstructive sleep apnea: a meta-analysis.0.0071770412013HTR2A1346895805GA
rs6313162582053358HTR2Cumls:C0520679BeFreeGenotypes and allele frequencies of 102T/C polymorphism of the HTR2A and 796G/C polymorphism of the HTR2C did not differ between controls and patients with OSA.0.0050055062005HTR2A1346895805GA
rs6520785219025981535CYBAumls:C0520679BeFreeThe frequencies of NADPH oxidase (NOX) polymorphisms in the p22phox subunit were similar between children with OSA and controls, except for rs6520785 and rs4673, the latter being significantly more frequent among the OSA children without deficits than with deficits (p<0.02).0.0031813582012CYBBX37785172CG
rs688845125660813133522PPARGC1Bumls:C0520679BeFreeIn peroxisome proliferator-activated receptor gamma, coactivator 1 beta (PPARGC1B), rs6888451 was associated with several markers of obstructive sleep apnea.0.0002714422014PPARGC1B5149744371CG,T
rs7030789231554145341PLEKumls:C0520679BeFreeUsing a panel of 46,449 polymorphisms from roughly 2,100 candidate genes on a customized Illumina iSelect chip, we tested for association with the apnea hypopnea index (AHI) as well as moderate to severe OSA (AHI≥15) in 3,551 participants of the Cleveland Family Study and two cohorts participating in the Sleep Heart Health Study.Among 647 African-Americans, rs11126184 in the pleckstrin (PLEK) gene was associated with OSA while rs7030789 in the lysophosphatidic acid receptor 1 (LPAR1) gene was associated with AHI using a chip-wide significance threshold of p-value<2×10(-6).0.0002714422012LPAR19110973232AG
rs7030789231554141902LPAR1umls:C0520679BeFreeUsing a panel of 46,449 polymorphisms from roughly 2,100 candidate genes on a customized Illumina iSelect chip, we tested for association with the apnea hypopnea index (AHI) as well as moderate to severe OSA (AHI≥15) in 3,551 participants of the Cleveland Family Study and two cohorts participating in the Sleep Heart Health Study.Among 647 African-Americans, rs11126184 in the pleckstrin (PLEK) gene was associated with OSA while rs7030789 in the lysophosphatidic acid receptor 1 (LPAR1) gene was associated with AHI using a chip-wide significance threshold of p-value<2×10(-6).0.0002714422012LPAR19110973232AG
rs9526240205389603356HTR2Aumls:C0520679BeFreeIn African Americans, rs9526240 within serotonin receptor 2a (HTR2A: odds ratio = 2.1; 95% confidence interval, 1.5-2.9; P = 0.00005233) was associated with OSA.0.0071770412010HTR2A1346857336GA
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
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Mapped by lexical matching(Total Items:0)
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Mapped by homologous gene(Total Items:0)
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Chemical(Total Drugs:5)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0520679cerivastatinC086276-sleep apnea, obstructiveMESH:D020181marker/mechanism18595439
C0520679enalaprilD00465675847-73-3sleep apnea, obstructiveMESH:D020181marker/mechanism16438479
C0520679montelukastC093875158966-92-8sleep apnea, obstructiveMESH:D020181therapeutic19118273
C0520679morphineD00902057-27-2sleep apnea, obstructiveMESH:D020181marker/mechanism2334618
C0520679spironolactoneD0131481952/1/7sleep apnea, obstructiveMESH:D020181therapeutic20016520
FDA approved drug and dosage information(Total Drugs:0)
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FDA labeling changes(Total Drugs:0)
(Waiting for update.)