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Details
Link-It Detail - Disease - Gallbladder Diseases
Debug Stats
  • ### Total Build Time: 379 ms 37.429 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 ms rowSize= 338 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 393 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=19 ms Completed: 19 ms rowSize= 558 bytes
  • CONCEPT_CHILDREN gt=12 ms Completed: 12 ms rowSize= 1.395 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=10 ms Completed: 10 ms rowSize= 1.517 KB
  • CONCEPT_RELATIONSHIPS gt=279 ms Completed: 279 ms rowSize= 14.113 KB
  • CONCEPT_GENES gt=43 ms Completed: 43 ms rowSize= 17.780 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.154 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Gallbladder Diseases C0016977
Definition (1)
condition in which there is a deviation from or interruption of the normal structure or function of the gallbladder; generally involves the impairment of bile flow, gallstones in the biliary tract, infections, neoplasms, or other diseases.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Biliary Tract Diseases C0005424
Children (3)
img Cholecystolithiasis C0947622
img Gallbladder Neoplasms C0016978
img Cholecystitis C0008325
Ancestral Roots
RootRoot Plus OneDepthParent
img Digestive System Diseases C0012242img Biliary Tract Diseases C00054243img Biliary Tract Diseases C0005424
Relationships (97)

Relation Types:
diso_​to_​anat : 11
diso_​to_​chem : 16
diso_​to_​diso : 68
diso_​to_​phen : 1
diso_​to_​phys : 1


Relationships:
none : 36
associated_​with : 1
classifies : 2
expanded_​form_​of : 1
is_​associated_​anatomic_​site_​of : 3
isa : 29
location_​of : 1
mapped_​to : 4
may_​diagnose : 16
related_​to : 4
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO94img Complication Aspects C1171258
DISO_to_DISO64img Complication Aspects C1171258
DISO_to_ANAT54img Gallbladder C0016976
DISO_to_ANAT41img Gallbladder C0016976
DISO_to_DISO41img Polyps C0032584
DISO_to_DISO25img Gallbladder Neoplasms C0016978
DISO_to_DISO24img Torsion Abnormality C1956418
DISO_to_DISO21img Bile duct fistula C0005417
DISO_to_DISO20img Choristoma C0008519
DISO_to_DISO18img Bile duct fistula C0005417
DISO_to_DISO18img Intestinal Fistula C0021833
DISO_to_DISO16img Intestinal Fistula C0021833
DISO_to_DISO16img Polyps C0032584
DISO_to_ANAT15img Biliary calculi C0242216
DISO_to_DISO15img Calcinosis C0006663
DISO_to_DISO15img Gallbladder Neoplasms C0016978
DISO_to_DISO15img Liver Diseases C0023895
DISO_to_DISO14img Cholecystitis C0008325
DISO_to_DISO13img Cholelithiasis C0008350
DISO_to_DISO13img Choristoma C0008519
DISO_to_ANAT12img Bile Ducts C0005400
DISO_to_ANAT12img Pancreas C0030274
DISO_to_DISO12img Calcinosis C0006663
DISO_to_DISO12img Cholelithiasis C0008350
DISO_to_ANAT11img Bile C0005388
Genes (74)

Species:
human : 74
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanOSTalpha200931
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanOSTBETA123264
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanABCG864241ATP-binding cassette, sub-family G (WHITE), member 8
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanABCG564240ATP-binding cassette, sub-family G (WHITE), member 5
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanUGT1A154658UDP glucuronosyltransferase 1 family, polypeptide A1
img GENERIF, Score=1000, Pubmed Id: 18756540, UMLKSK CUI: C0016977
HumanSH3GLB151100SH3-domain GRB2-like endophilin B1
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanNPC1L129881NPC1-like 1
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanNR1H49971nuclear receptor subfamily 1, group H, member 4
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanKEAP19817kelch-like ECH-associated protein 1
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanCLDN29075claudin 2
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanCES28824carboxylesterase 2
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanABCB118647ATP-binding cassette, sub-family B (MDR/TAP), member 11
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanCUBN8029cubilin (intrinsic factor-cobalamin receptor)
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanVIPR27434vasoactive intestinal peptide receptor 2
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanVIP7432vasoactive intestinal peptide
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanVEGFC7424vascular endothelial growth factor C
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanTP537157tumor protein p53
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanTOP2A7153topoisomerase (DNA) II alpha 170kDa
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanTNF7124tumor necrosis factor
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanTGFB17040transforming growth factor, beta 1
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanTBX16899T-box 1
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanSLC10A26555solute carrier family 10 (sodium/bile acid cotransporter), member 2
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanPRLR5618prolactin receptor
INFERRED, Score=800, UMLKSK CUI: C0016977
HumanPPARG5468peroxisome proliferator-activated receptor gamma
INFERRED, Score=800, UMLKSK CUI: C0016977
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0016977Gallbladder Diseases0self