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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   gallbladder disease
  

Disease ID 1322
Disease gallbladder disease
Definition
Diseases of the GALLBLADDER. They generally involve the impairment of BILE flow, GALLSTONES in the BILIARY TRACT, infections, neoplasms, or other diseases.
Synonym
biliary disease
biliary diseases
bladder disease, gall
bladder diseases, gall
dis of gallbladder nos
disease biliary
disease gallbladder
disease of gallbladder
disease of gallbladder (disorder)
disease of gallbladder, nos
disease, gall bladder
disease, gallbladder
diseases, gall bladder
diseases, gallbladder
disorder of gallbladder
disorder of gallbladder (disorder)
gall bladder dis
gall bladder disease
gall bladder diseases
gall bladder disorder
gall bladder disorders nos
gallbladder dis
gallbladder diseases
gallbladder diseases [disease/finding]
gallbladder disorder
gallbladder disorder, nos
gallbladder disorders
gallbladder disorders nos
gallbladder disorders nos (disorder)
gallbladder--diseases
unspecified disorder of gallbladder
DOID
UMLS
C0016977
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:23)
C0030305  |  pancreatitis  |  3
C0008325  |  cholecystitis  |  2
C0001339  |  acute pancreatitis  |  2
C0023890  |  cirrhosis  |  2
C0019322  |  umbilical hernia  |  1
C0153452  |  gallbladder cancer  |  1
C0376358  |  prostate cancer  |  1
C0007222  |  cardiovascular disease  |  1
C0005684  |  bladder cancer  |  1
C0011847  |  diabetes  |  1
C0008350  |  cholelithiasis  |  1
C0011860  |  type 2 diabetes  |  1
C0011860  |  type 2 diabetes mellitus  |  1
C0153452  |  gallbladder ca  |  1
C0023890  |  liver cirrhosis  |  1
C0019204  |  hepatocellular carcinoma  |  1
C0042373  |  vascular disease  |  1
C0023895  |  liver disease  |  1
C0011570  |  depression  |  1
C0037661  |  somatostatinoma  |  1
C0029408  |  osteoarthritis  |  1
C0005398  |  extrahepatic biliary obstruction  |  1
C0029106  |  opisthorchiasis  |  1
Curated Gene(Waiting for update.)
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:15)
91526  |  ANKRD44  |  CIPHER
338  |  APOB  |  CIPHER
348  |  APOE  |  CIPHER
1803  |  DPP4  |  CIPHER
8087  |  FXR1  |  CIPHER
266722  |  HS6ST3  |  CIPHER
8690  |  JRKL  |  CIPHER
359750  |  MRPL50P3  |  CIPHER
50863  |  NTM  |  CIPHER
11122  |  PTPRT  |  CIPHER
5898  |  RALA  |  CIPHER
100271352  |  RPS12P16  |  CIPHER
387495  |  RPS26P5  |  CIPHER
6555  |  SLC10A2  |  CIPHER
25769  |  SLC24A2  |  CIPHER
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:89)
1244  |  ABCC2  |  1.02  |  DISEASES
58  |  ACTA1  |  1.19  |  DISEASES
174  |  AFP  |  1.285  |  DISEASES
119016  |  AGAP4  |  4.027  |  DISEASES
414189  |  AGAP6  |  4.027  |  DISEASES
642517  |  AGAP9  |  4.027  |  DISEASES
336  |  APOA2  |  1.595  |  DISEASES
9138  |  ARHGEF1  |  1.763  |  DISEASES
438  |  ASMT  |  1.48  |  DISEASES
522  |  ATP5J  |  1.022  |  DISEASES
801  |  CALM1  |  1.014  |  DISEASES
885  |  CCK  |  6.429  |  DISEASES
56477  |  CCL28  |  1.791  |  DISEASES
959  |  CD40LG  |  1.674  |  DISEASES
146059  |  CDAN1  |  1.189  |  DISEASES
23436  |  CELA3B  |  2.337  |  DISEASES
9557  |  CHD1L  |  1.859  |  DISEASES
7180  |  CRISP2  |  2.201  |  DISEASES
1504  |  CTRB1  |  2.059  |  DISEASES
192668  |  CYS1  |  1.007  |  DISEASES
1854  |  DUT  |  1.322  |  DISEASES
2152  |  F3  |  2.18  |  DISEASES
2172  |  FABP6  |  2.379  |  DISEASES
84293  |  FAM213A  |  2.179  |  DISEASES
2235  |  FECH  |  1.941  |  DISEASES
2316  |  FLNA  |  1.179  |  DISEASES
2520  |  GAST  |  3.1  |  DISEASES
2641  |  GCG  |  2.605  |  DISEASES
2673  |  GFPT1  |  1.26  |  DISEASES
728441  |  GGT2  |  2.968  |  DISEASES
151306  |  GPBAR1  |  1.943  |  DISEASES
2859  |  GPR35  |  1.663  |  DISEASES
57000  |  GSN-AS1  |  1.524  |  DISEASES
3030  |  HADHA  |  2.608  |  DISEASES
3043  |  HBB  |  2.577  |  DISEASES
3045  |  HBD  |  1.244  |  DISEASES
3055  |  HCK  |  1.336  |  DISEASES
3068  |  HDGF  |  1.053  |  DISEASES
84525  |  HOPX  |  1.088  |  DISEASES
3240  |  HP  |  1.502  |  DISEASES
7866  |  IFRD2  |  2.554  |  DISEASES
3486  |  IGFBP3  |  1.001  |  DISEASES
3633  |  INPP5B  |  1.702  |  DISEASES
102723508  |  KANTR  |  3.145  |  DISEASES
3855  |  KRT7  |  1.025  |  DISEASES
3953  |  LEPR  |  1.399  |  DISEASES
4018  |  LPA  |  2.524  |  DISEASES
9404  |  LPXN  |  2.411  |  DISEASES
4047  |  LSS  |  1.066  |  DISEASES
4146  |  MATN1  |  1.092  |  DISEASES
57708  |  MIER1  |  1.356  |  DISEASES
4295  |  MLN  |  2.383  |  DISEASES
4583  |  MUC2  |  1.094  |  DISEASES
4586  |  MUC5AC  |  1.416  |  DISEASES
4588  |  MUC6  |  1.044  |  DISEASES
25915  |  NDUFAF3  |  1.927  |  DISEASES
283820  |  NOMO2  |  1.5  |  DISEASES
408050  |  NOMO3  |  1.503  |  DISEASES
9971  |  NR1H4  |  2.995  |  DISEASES
2494  |  NR5A2  |  1.759  |  DISEASES
5095  |  PCCA  |  1.064  |  DISEASES
80012  |  PHC3  |  1.289  |  DISEASES
5362  |  PLXNA2  |  1.506  |  DISEASES
5407  |  PNLIPRP1  |  2.463  |  DISEASES
56980  |  PRDM10  |  1.068  |  DISEASES
9939  |  RBM8A  |  1.756  |  DISEASES
23212  |  RRS1  |  1.453  |  DISEASES
6280  |  S100A9  |  2.589  |  DISEASES
6303  |  SAT1  |  2.052  |  DISEASES
5265  |  SERPINA1  |  1.007  |  DISEASES
145264  |  SERPINA12  |  1.423  |  DISEASES
462  |  SERPINC1  |  2.372  |  DISEASES
9356  |  SLC22A6  |  1.105  |  DISEASES
123264  |  SLC51B  |  1.73  |  DISEASES
23583  |  SMUG1  |  1.43  |  DISEASES
6752  |  SSTR2  |  1.186  |  DISEASES
26136  |  TES  |  2.077  |  DISEASES
51337  |  THEM6  |  1.238  |  DISEASES
7124  |  TNF  |  1.759  |  DISEASES
27095  |  TRAPPC3  |  2.021  |  DISEASES
158219  |  TTC39B  |  2.718  |  DISEASES
27229  |  TUBGCP4  |  1.463  |  DISEASES
54575  |  UGT1A10  |  1.302  |  DISEASES
54659  |  UGT1A3  |  1.231  |  DISEASES
54576  |  UGT1A8  |  1.294  |  DISEASES
7405  |  UVRAG  |  1.438  |  DISEASES
7432  |  VIP  |  2.058  |  DISEASES
400673  |  VMAC  |  2.509  |  DISEASES
7633  |  ZNF79  |  2.392  |  DISEASES
Locus(Waiting for update.)
Disease ID 1322
Disease gallbladder disease
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:19)
HP:0001733  |  Pancreatic inflammation  |  3
HP:0001394  |  Hepatic cirrhosis  |  2
HP:0001513  |  Obesity  |  2
HP:0001735  |  Acute pancreatitis  |  2
HP:0001082  |  Cholecystitis  |  2
HP:0001399  |  Liver failure  |  1
HP:0002664  |  Neoplasia  |  1
HP:0003077  |  Hyperlipidemia  |  1
HP:0009725  |  Bladder neoplasm  |  1
HP:0001510  |  Growth deficiency  |  1
HP:0001402  |  Hepatocellular carcinoma  |  1
HP:0100806  |  Sepsis  |  1
HP:0012125  |  Prostate cancer  |  1
HP:0004800  |  Duodenal diverticula  |  1
HP:0002758  |  Osteoarthritis  |  1
HP:0000716  |  Depression  |  1
HP:0100790  |  Hernia  |  1
HP:0001081  |  Gallstones  |  1
HP:0001537  |  Umbilical hernias  |  1
Disease ID 1322
Disease gallbladder disease
Manually Symptom
UMLS  | Name(Total Manually Symptoms:4)
C2598155  |  pain
C1963198  |  pancreatitis
C0422833  |  ent symptoms
C0162871  |  abdominal aortic aneurysm
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:4)
C0009450  |  infection  |  4
C0030305  |  pancreatitis  |  3
C0001339  |  acute pancreatitis  |  2
C0019204  |  hepatocellular carcinoma  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total 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.)
Disease ID 1322
Disease gallbladder disease
Case(Waiting for update.)