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Pediatric Disease Annotations & Medicines



   gastroparesis
  

Disease ID 833
Disease gastroparesis
Definition
Chronic delayed gastric emptying. Gastroparesis may be caused by motor dysfunction or paralysis of STOMACH muscles or may be associated with other systemic diseases such as DIABETES MELLITUS.
Synonym
atony stomach
delayed gastric emptying
gastric atonia
gastric atonia (disorder)
gastric atony
gastric paralysis
gastric stases
gastric stasis
gastroparalysis
gastropareses
gastroparesis (disorder)
gastroparesis [disease/finding]
gastroparesis syndrome
gastroparesis syndrome (disorder)
gastroparesis syndrome (disorder) [ambiguous]
gastroparesis syndrome, nos
paralysis gastric
stases, gastric
stasis, gastric
stomach atony
DOID
ICD10
UMLS
C0152020
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:22)
C0011847  |  diabetes  |  17
C0011849  |  diabetes mellitus  |  7
C0003467  |  anxiety  |  2
C0011860  |  type 2 diabetes  |  2
C0023890  |  cirrhosis  |  2
C0023890  |  liver cirrhosis  |  2
C0011854  |  type 1 diabetes  |  2
C0011854  |  type 1 diabetes mellitus  |  2
C0030567  |  parkinson's disease  |  2
C0001173  |  gastric outlet obstruction  |  1
C0442874  |  neuropathy  |  1
C0011880  |  diabetic ketoacidosis  |  1
C0751651  |  mitochondrial disorder  |  1
C0001418  |  adenocarcinoma  |  1
C0162429  |  poor nutrition  |  1
C0009319  |  colitis  |  1
C0011570  |  depression  |  1
C0038353  |  gastric dilatation  |  1
C0017178  |  gastrointestinal disorders  |  1
C0017178  |  gastrointestinal disorder  |  1
C0035309  |  retinopathy  |  1
C0259749  |  autonomic neuropathy  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
HMOX1  |  3162  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:10)
5243  |  ABCB1  |  infer
148  |  ADRA1A  |  infer
147  |  ADRA1B  |  infer
146  |  ADRA1D  |  infer
1565  |  CYP2D6  |  infer
1813  |  DRD2  |  infer
3753  |  KCNE1  |  infer
9992  |  KCNE2  |  infer
3757  |  KCNH2  |  infer
3784  |  KCNQ1  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:95)
10573  |  MRPL28  |  DISEASES
28954  |  REM1  |  DISEASES
9552  |  SPAG7  |  DISEASES
3162  |  HMOX1  |  DISEASES
479  |  ATP12A  |  DISEASES
2862  |  MLNR  |  DISEASES
5216  |  PFN1  |  DISEASES
5539  |  PPY  |  DISEASES
4254  |  KITLG  |  DISEASES
2729  |  GCLC  |  DISEASES
5754  |  PTK7  |  DISEASES
8574  |  AKR7A2  |  DISEASES
4360  |  MRC1  |  DISEASES
2693  |  GHSR  |  DISEASES
8189  |  SYMPK  |  DISEASES
7166  |  TPH1  |  DISEASES
3630  |  INS  |  DISEASES
384  |  ARG2  |  DISEASES
3757  |  KCNH2  |  DISEASES
495  |  ATP4A  |  DISEASES
25939  |  SAMHD1  |  DISEASES
126374  |  WTIP  |  DISEASES
3782  |  KCNN3  |  DISEASES
90226  |  UCN2  |  DISEASES
2746  |  GLUD1  |  DISEASES
6327  |  SCN2B  |  DISEASES
7345  |  UCHL1  |  DISEASES
6750  |  SST  |  DISEASES
3815  |  KIT  |  DISEASES
9992  |  KCNE2  |  DISEASES
6285  |  S100B  |  DISEASES
114757  |  CYGB  |  DISEASES
4880  |  NPPC  |  DISEASES
886  |  CCKAR  |  DISEASES
213  |  ALB  |  DISEASES
94274  |  PPP1R14A  |  DISEASES
2353  |  FOS  |  DISEASES
147  |  ADRA1B  |  DISEASES
3352  |  HTR1D  |  DISEASES
619373  |  MBOAT4  |  DISEASES
3350  |  HTR1A  |  DISEASES
147912  |  SIX5  |  DISEASES
8630  |  HSD17B6  |  DISEASES
6863  |  TAC1  |  DISEASES
64840  |  PORCN  |  DISEASES
7485  |  WRB  |  DISEASES
8905  |  AP1S2  |  DISEASES
4105  |  MAGEA6  |  DISEASES
8519  |  IFITM1  |  DISEASES
2520  |  GAST  |  DISEASES
3751  |  KCND2  |  DISEASES
51738  |  GHRL  |  DISEASES
885  |  CCK  |  DISEASES
1103  |  CHAT  |  DISEASES
4842  |  NOS1  |  DISEASES
3363  |  HTR7  |  DISEASES
54468  |  MIOS  |  DISEASES
80320  |  SP6  |  DISEASES
4882  |  NPR2  |  DISEASES
259307  |  IL4I1  |  DISEASES
55107  |  ANO1  |  DISEASES
3359  |  HTR3A  |  DISEASES
6525  |  SMTN  |  DISEASES
5697  |  PYY  |  DISEASES
3360  |  HTR4  |  DISEASES
1813  |  DRD2  |  DISEASES
28514  |  DLL1  |  DISEASES
7432  |  VIP  |  DISEASES
4881  |  NPR1  |  DISEASES
2730  |  GCLM  |  DISEASES
23413  |  NCS1  |  DISEASES
51230  |  PHF20  |  DISEASES
1041  |  CDSN  |  DISEASES
1804  |  DPP6  |  DISEASES
146  |  ADRA1D  |  DISEASES
114131  |  UCN3  |  DISEASES
7054  |  TH  |  DISEASES
1814  |  DRD3  |  DISEASES
9290  |  GPR55  |  DISEASES
100131390  |  SP9  |  DISEASES
594857  |  NPS  |  DISEASES
643418  |  LIPN  |  DISEASES
2115  |  ETV1  |  DISEASES
2641  |  GCG  |  DISEASES
4295  |  MLN  |  DISEASES
5817  |  PVR  |  DISEASES
221833  |  SP8  |  DISEASES
51227  |  PIGP  |  DISEASES
149466  |  C1orf210  |  DISEASES
56  |  ACRV1  |  DISEASES
5125  |  PCSK5  |  DISEASES
102723508  |  KANTR  |  DISEASES
103752588  |  PACERR  |  DISEASES
692149  |  SCARNA14  |  DISEASES
100128252  |  ZNF667-AS1  |  DISEASES
Locus(Waiting for update.)
Disease ID 833
Disease gastroparesis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:16)
HP:0002018  |  Nausea  |  9
HP:0002013  |  Emesis  |  8
HP:0002017  |  Nausea and vomiting  |  7
HP:0000819  |  Diabetes mellitus  |  7
HP:0002578  |  Gastroparesis  |  5
HP:0002835  |  Aspiration  |  2
HP:0001394  |  Hepatic cirrhosis  |  2
HP:0000739  |  Anxiety  |  2
HP:0012531  |  Pain  |  1
HP:0001993  |  Ketoacidosis  |  1
HP:0012378  |  Fatigue  |  1
HP:0000488  |  Noninflammatory retina disease  |  1
HP:0001953  |  Diabetic ketosis  |  1
HP:0000716  |  Depression  |  1
HP:0001944  |  Dehydration  |  1
HP:0002583  |  Colitis  |  1
Disease ID 833
Disease gastroparesis
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:7)
C0027497  |  nausea  |  9
C0042963  |  vomiting  |  8
C0011849  |  diabetes mellitus  |  7
C0003467  |  anxiety  |  2
C0750323  |  intractable vomiting  |  1
C0011570  |  depression  |  1
C0030193  |  pain  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:2)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0152020cisaprideD02011781098-60-4gastroparesisMESH:D018589therapeutic11578711
C0152020vincristineD014750-gastroparesisMESH:D018589marker/mechanism19448908
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)