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Pediatric Disease Annotations & Medicines



   motion sickness
  

Disease ID 488
Disease motion sickness
Definition
Disorder caused by motion, as sea sickness, train sickness, car sickness, air sickness, or SPACE MOTION SICKNESS. It may include nausea, vomiting and dizziness.
Synonym
motion sickness (disorder)
motion sickness (finding)
motion sickness [disease/finding]
motion sickness nos
motion sickness nos (disorder)
motion sickness nos (finding)
motion sickness, nos
riders' vertigo
sickness, motion
travel sickness
travel sickness (disorder)
travel sickness, unspecified
travel sickness, unspecified (disorder)
travel sickness, unspecified (finding)
OMIM
DOID
UMLS
C0026603
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:10)
C0149931  |  migraine  |  6
C0028754  |  obesity  |  5
C0021831  |  intestinal disease  |  1
C0037274  |  skin disease  |  1
C0020538  |  hypertension  |  1
C0003615  |  appendicitis  |  1
C0017178  |  gastrointestinal disease  |  1
C0008311  |  cholangitis  |  1
C0011847  |  diabetes  |  1
C0003467  |  anxiety  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:17)
CELF2  |  10659  |  GWASCAT
MAP2K5  |  5607  |  GWASCAT
NLGN1  |  22871  |  GWASCAT
AUTS2  |  26053  |  GWASCAT
LINC00924  |  145820  |  GWASCAT
PRDM16  |  63976  |  GWASCAT
LRP1B  |  53353  |  GWASCAT
HOXB3  |  3213  |  GWASCAT
POU6F2  |  11281  |  GWASCAT
LINC01243  |  101929620  |  GWASCAT
LINC01241  |  101929582  |  GWASCAT
GPD2  |  2820  |  GWASCAT
HOXD3  |  3232  |  GWASCAT
SDK1  |  221935  |  GWASCAT
ST18  |  9705  |  GWASCAT
CPNE4  |  131034  |  GWASCAT
PDZRN4  |  29951  |  GWASCAT
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:1)
150  |  ADRA2A  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:97)
84908  |  FAM136A  |  DISEASES
4320  |  MMP11  |  DISEASES
1690  |  COCH  |  DISEASES
55916  |  NXT2  |  DISEASES
1577  |  CYP3A5  |  DISEASES
5539  |  PPY  |  DISEASES
4848  |  CNOT2  |  DISEASES
56269  |  IRGC  |  DISEASES
3232  |  HOXD3  |  DISEASES
10053  |  AP1M2  |  DISEASES
9360  |  PPIG  |  DISEASES
9132  |  KCNQ4  |  DISEASES
8540  |  AGPS  |  DISEASES
5443  |  POMC  |  DISEASES
11343  |  MGLL  |  DISEASES
6895  |  TARBP2  |  DISEASES
60314  |  C12orf10  |  DISEASES
5972  |  REN  |  DISEASES
3358  |  HTR2C  |  DISEASES
90525  |  SHF  |  DISEASES
1173  |  AP2M1  |  DISEASES
4041  |  LRP5  |  DISEASES
152185  |  SPICE1  |  DISEASES
84315  |  MON1A  |  DISEASES
364  |  AQP7  |  DISEASES
5617  |  PRL  |  DISEASES
6869  |  TACR1  |  DISEASES
2353  |  FOS  |  DISEASES
3213  |  HOXB3  |  DISEASES
1657  |  DMXL1  |  DISEASES
171389  |  NLRP6  |  DISEASES
358  |  AQP1  |  DISEASES
3352  |  HTR1D  |  DISEASES
3350  |  HTR1A  |  DISEASES
57217  |  TTC7A  |  DISEASES
64388  |  GREM2  |  DISEASES
363  |  AQP6  |  DISEASES
10938  |  EHD1  |  DISEASES
6863  |  TAC1  |  DISEASES
10194  |  TSHZ1  |  DISEASES
51341  |  ZBTB7A  |  DISEASES
131149  |  OTOL1  |  DISEASES
2520  |  GAST  |  DISEASES
5797  |  PTPRM  |  DISEASES
25987  |  TSKU  |  DISEASES
9939  |  RBM8A  |  DISEASES
51738  |  GHRL  |  DISEASES
327657  |  SERPINA9  |  DISEASES
1576  |  CYP3A4  |  DISEASES
3363  |  HTR7  |  DISEASES
2261  |  FGFR3  |  DISEASES
222236  |  NAPEPLD  |  DISEASES
6609  |  SMPD1  |  DISEASES
9588  |  PRDX6  |  DISEASES
9536  |  PTGES  |  DISEASES
1811  |  SLC26A3  |  DISEASES
2879  |  GPX4  |  DISEASES
3792  |  KEL  |  DISEASES
3359  |  HTR3A  |  DISEASES
3360  |  HTR4  |  DISEASES
1118  |  CHIT1  |  DISEASES
7432  |  VIP  |  DISEASES
1268  |  CNR1  |  DISEASES
4803  |  NGF  |  DISEASES
1137  |  CHRNA4  |  DISEASES
26036  |  ZNF451  |  DISEASES
26027  |  ACOT11  |  DISEASES
6406  |  SEMG1  |  DISEASES
9968  |  MED12  |  DISEASES
1269  |  CNR2  |  DISEASES
2159  |  F10  |  DISEASES
79180  |  EFHD2  |  DISEASES
127262  |  TPRG1L  |  DISEASES
3980  |  LIG3  |  DISEASES
551  |  AVP  |  DISEASES
5618  |  PRLR  |  DISEASES
3786  |  KCNQ3  |  DISEASES
2524  |  FUT2  |  DISEASES
6046  |  BRD2  |  DISEASES
2132  |  EXT2  |  DISEASES
3269  |  HRH1  |  DISEASES
63915  |  BLOC1S5  |  DISEASES
1837  |  DTNA  |  DISEASES
643418  |  LIPN  |  DISEASES
7514  |  XPO1  |  DISEASES
1385  |  CREB1  |  DISEASES
4295  |  MLN  |  DISEASES
4988  |  OPRM1  |  DISEASES
6464  |  SHC1  |  DISEASES
64084  |  CLSTN2  |  DISEASES
4152  |  MBD1  |  DISEASES
627  |  BDNF  |  DISEASES
246744  |  STH  |  DISEASES
5125  |  PCSK5  |  DISEASES
8972  |  MGAM  |  DISEASES
5726  |  TAS2R38  |  DISEASES
101  |  ADAM8  |  DISEASES
Locus(Waiting for update.)
Disease ID 488
Disease motion sickness
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:1)
HP:0000707  |  Neurological abnormality
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:13)
HP:0002018  |  Nausea  |  10
HP:0002013  |  Emesis  |  10
HP:0002076  |  Migraine headaches  |  6
HP:0001513  |  Obesity  |  5
HP:0002017  |  Nausea and vomiting  |  4
HP:0100785  |  Insomnia  |  1
HP:0030151  |  Cholangitis  |  1
HP:0001751  |  Vestibular dysfunction  |  1
HP:0000822  |  Hypertension  |  1
HP:0000708  |  Behavioral problems  |  1
HP:0001824  |  Weight loss  |  1
HP:0000739  |  Anxiety  |  1
HP:0002172  |  Postural instability  |  1
Disease ID 488
Disease motion sickness
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:3)
C0027497  |  nausea  |  10
C0042963  |  vomiting  |  9
C0231218  |  malaise  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:19)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs107522122562833610659CELF2umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015NA1010875158GA
rs1097030525628336101929620LINC01243umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015LINC01243931372585AC
rs117131692562833622871NLGN1umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015NLGN13173666799AC
rs175152252562833653353LRP1Bumls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015LRP1B2140788186TC
rs178203225628336101929582LINC01241umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015LINC01241925804287AG
rs2360806256283369705ST18umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015ST18852213174AC
rs2551802256283363232HOXD3umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015HOXD32176157430CG
rs343112352562833653353LRP1Bumls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015LRP1B2142009864CT
rs3491221625628336221935SDK1umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015SDK174078745GA
rs434399625628336221935SDK1umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015SDK173323010GA
rs56051278256283362820GPD2umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015GPD22156525242AG
rs604640472562833611281POU6F2umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015POU6F2739378939TA
rs617591672562833663976PRDM16umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015PRDM1613175023CT
rs69469692562833626053AUTS2umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015AUTS2;LOC105375347770746041GA
rs717066825628336145820LINC00924umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015LINC00924;LOC1053709931595470914TC
rs79575892562833629951PDZRN4umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015PDZRN41241480480AT
rs983456025628336131034CPNE4umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015CPNE4;LOC1053741123131997261CA
rs9906289256283363213HOXB3umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015HOXB31748567315CT
rs997295256283365607MAP2K5umls:C0026603GWASCATGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.0.122015MAP2K51567724005GT
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:1)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0026603nicotineD009538-motion sicknessMESH:D009041marker/mechanism17990061
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)