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Details
Link-It Detail - Disease - Esophageal Diseases
Debug Stats
  • ### Total Build Time: 100 ms 44.514 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 336 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 194 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=0 Completed: 0 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 561 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 4.825 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.522 KB
  • CONCEPT_RELATIONSHIPS gt=68 ms Completed: 68 ms rowSize= 14.352 KB
  • CONCEPT_GENES gt=27 ms Completed: 27 ms rowSize= 21.385 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Esophageal Diseases C0014852
Definition (1)
Pathological processes in the ESOPHAGUS.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Gastrointestinal Diseases C0017178
Children (11)
img Esophageal Neoplasms C0014859
img Esophageal Perforation C0014860
img Esophageal Atresia C0014850
img Esophageal and Gastric Varices C0014849
img Diverticulosis, Esophageal C0917875
img Esophageal Cyst C0014851
img Deglutition Disorders C0011168
img Esophageal Stenosis C0014866
img Esophagitis C0014868
img Barrett Esophagus C0004763
img Esophageal Fistula C0014856
Ancestral Roots
RootRoot Plus OneDepthParent
img Digestive System Diseases C0012242img Gastrointestinal Diseases C00171783img Gastrointestinal Diseases C0017178
Relationships (212)

Relation Types:
diso_​to_​anat : 12
diso_​to_​chem : 91
diso_​to_​diso : 109


Relationships:
none : 55
associated_​with : 1
classified_​as : 15
classifies : 1
is_​associated_​anatomic_​site_​of : 2
isa : 39
mapped_​to : 8
may_​diagnose : 55
may_​treat : 33
related_​to : 2
use : 1
Page Size
Current 25
  Page 1 of 9
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT125img Esophagus C0014876
DISO_to_DISO119img Complication Aspects C1171258
DISO_to_DISO96img Complication Aspects C1171258
DISO_to_ANAT71img Esophagus C0014876
DISO_to_DISO45img Ulcer C0041582
DISO_to_DISO40img Choristoma C0008519
DISO_to_DISO40img Stomach Diseases C0038354
DISO_to_DISO36img chemically induced C0007994
DISO_to_ANAT31img Gastric Mucosa C0017136
DISO_to_DISO31img chemically induced C0007994
DISO_to_DISO30img Deglutition Disorders C0011168
DISO_to_DISO30img Hematoma C0018944
DISO_to_DISO29img BLEEDING GASTROINTESTINAL C0017181
DISO_to_DISO26img Deglutition Disorders C0011168
DISO_to_DISO26img Esophageal Neoplasms C0014859
DISO_to_DISO25img Choristoma C0008519
DISO_to_DISO24img Candidiasis C0006840
DISO_to_DISO24img Polyps C0032584
DISO_to_DISO24img Stomach Diseases C0038354
DISO_to_ANAT21img Esophagogastric Junction C0014871
DISO_to_ANAT21img Gastric Mucosa C0017136
DISO_to_DISO19img COMPL POSTOP C0032787
DISO_to_DISO19img Esophageal Neoplasms C0014859
DISO_to_DISO18img BLEEDING GASTROINTESTINAL C0017181
DISO_to_DISO18img Polyps C0032584
Genes (296)

Species:
human : 296
Page Size
Current 25
  Page 1 of 12
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCSAG2728461CSAG family, member 2
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanMIR196A1406972microRNA 196a-1
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanVSIG1340547V-set and immunoglobulin domain containing 1
img GENERIF, Score=861, Pubmed Id: 16405301, UMLKSK CUI: C0014852
HumanTMPRSS11A339967transmembrane protease, serine 11A
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanARX170302aristaless related homeobox
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanGATA5140628GATA binding protein 5
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanMMP21118856matrix metallopeptidase 21
img GENERIF, Score=694, Pubmed Id: 16641547, UMLKSK CUI: C0014852
HumanEMILIN390187elastin microfibril interfacer 3
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanC15orf4884419chromosome 15 open reading frame 48
img GENERIF, Score=694, Pubmed Id: 12209954, UMLKSK CUI: C0014852
HumanC2orf4084417chromosome 2 open reading frame 40
img GENERIF, Score=804, Pubmed Id: 17786363, UMLKSK CUI: C0014852
HumanPDCD1LG280380programmed cell death 1 ligand 2
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanSPG1180208spastic paraplegia 11 (autosomal recessive)
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanRNF3480196ring finger protein 34, E3 ubiquitin protein ligase
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanPANK280025pantothenate kinase 2
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanWNK165125WNK lysine deficient protein kinase 1
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanRSRC265117arginine/serine-rich coiled-coil 2
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanIL2159067interleukin 21
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanADAMTS956999ADAM metallopeptidase with thrombospondin type 1 motif, 9
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanCHFR55743checkpoint with forkhead and ring finger domains, E3 ubiquitin protein ligase
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanCHD755636chromodomain helicase DNA binding protein 7
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanNOP1055505NOP10 ribonucleoprotein
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanPDP154704pyruvate dehyrogenase phosphatase catalytic subunit 1
INFERRED, Score=800, UMLKSK CUI: C0014852
HumanKRT2054474keratin 20
img GENERIF, Score=1000, Pubmed Id: 14631371, UMLKSK CUI: C0014852
HumanLRP1B53353low density lipoprotein receptor-related protein 1B
img GENERIF, Score=812, Pubmed Id: 15172977, UMLKSK CUI: C0014852
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0014852Esophageal Diseases0self