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) |
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.) |