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Details
Link-It Detail - Disease - Fistula
Debug Stats
  • ### Total Build Time: 89 ms 41.895 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 312 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 531 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= 247 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 571 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 3.099 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.560 KB
  • CONCEPT_RELATIONSHIPS gt=65 ms Completed: 65 ms rowSize= 12.943 KB
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 21.502 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.142 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Fistula C0016169
Definition (1)

A fistula is an abnormal connection between two parts inside of the body. Fistulas can happen because of injury, infection or inflammation. They may develop between different organs such as between the esophagus and the windpipe, or the bowel and the vagina. They can also develop between two blood vessels such as between an artery and a vein, or between two arteries.

Semantic Types (2)
Anatomical Abnormality (T190)
Pathologic Function (T046)
Parents (1)
img Pathological Conditions, Anatomical C0752135
Children (7)
img Vaginal Fistula C0042253
img Cutaneous Fistula C0423772
img Oral Fistula C0079943
img Digestive System Fistula C0079238
img Urinary Fistula C0042021
img Respiratory Tract Fistula C0080107
img Vascular Fistula C0080304
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Pathological Conditions, Anatomical C07521353img Pathological Conditions, Anatomical C0752135
Relationships (160)

Relation Types:
diso_​to_​anat : 21
diso_​to_​diso : 139


Relationships:
none : 77
isa : 79
mapped_​to : 3
parent_​is_​cdrh : 1
Page Size
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  Page 1 of 7
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Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO130img Complication Aspects C1171258
DISO_to_DISO105img Complication Aspects C1171258
DISO_to_DISO74img COMPL POSTOP C0032787
DISO_to_DISO74img Heart Diseases C0018799
DISO_to_DISO70img COMPL POSTOP C0032787
DISO_to_DISO55img Pleural Diseases C0032226
DISO_to_DISO53img Cutaneous Fistula C0423772
DISO_to_DISO44img Pleural Diseases C0032226
DISO_to_DISO41img 2-03 DISEASES OF THE PHARYNX C0031345
DISO_to_DISO39img Anomalies, Coronary Vessel C0010074
DISO_to_ANAT38img Heart Ventricle C0018827
DISO_to_DISO38img Esophageal Fistula C0014856
DISO_to_DISO36img 3-83 DISEASES OF THE AORTA C0003493
DISO_to_DISO34img BRONCHIAL FISTULA C0006262
DISO_to_DISO34img Labyrinth Diseases C0022890
DISO_to_DISO34img Uterine Diseases C0042131
DISO_to_ANAT33img Heart Atria C0018792
DISO_to_DISO32img Fistula, Vascular C0080304
DISO_to_DISO32img Heart Diseases C0018799
DISO_to_DISO32img Intestinal Fistula C0021833
DISO_to_DISO32img Labyrinth Diseases C0022890
DISO_to_DISO30img Fistula, Vascular C0080304
DISO_to_DISO30img Uterine Diseases C0042131
DISO_to_DISO29img 3-83 DISEASES OF THE AORTA C0003493
DISO_to_DISO27img Coronary Artery Disease C1956346
Genes (41)

Species:
human : 41
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMUC5B727897mucin 5B, oligomeric mucus/gel-forming
img GENERIF, Score=694, Pubmed Id: 17621824, UMLKSK CUI: C0016169
HumanIBD9317669inflammatory bowel disease 9
img OMIM, Score=1000, UMLKSK CUI: C0016169
HumanIBD8170595inflammatory bowel disease 8
img OMIM, Score=1000, UMLKSK CUI: C0016169
HumanIL23R149233interleukin 23 receptor
img OMIM, Score=1000, UMLKSK CUI: C0016169
HumanVANGL181839VANGL planar cell polarity protein 1
INFERRED, Score=800, UMLKSK CUI: C0016169
HumanNOD264127nucleotide-binding oligomerization domain containing 2
img OMIM, Score=1000, UMLKSK CUI: C0016169
HumanSALL457167sal-like 4 (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0016169
HumanIBD757042inflammatory bowel disease 7
img OMIM, Score=1000, UMLKSK CUI: C0016169
HumanCHD755636chromodomain helicase DNA binding protein 7
INFERRED, Score=800, UMLKSK CUI: C0016169
HumanAGGF155109angiogenic factor with G patch and FHA domains 1
INFERRED, Score=800, UMLKSK CUI: C0016169
HumanIBD650942inflammatory bowel disease 6
img OMIM, Score=1000, UMLKSK CUI: C0016169
HumanIBD550941inflammatory bowel disease 5
img OMIM, Score=1000, UMLKSK CUI: C0016169
HumanIBD450608inflammatory bowel disease 4
img OMIM, Score=1000, UMLKSK CUI: C0016169
HumanIBD330829inflammatory bowel disease 3
img OMIM, Score=1000, UMLKSK CUI: C0016169
HumanSEMA3E9723sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
INFERRED, Score=800, UMLKSK CUI: C0016169
HumanRECQL49401RecQ protein-like 4
INFERRED, Score=800, UMLKSK CUI: C0016169
HumanDLG59231discs, large homolog 5 (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0016169
HumanMKKS8195McKusick-Kaufman syndrome
INFERRED, Score=800, UMLKSK CUI: C0016169
HumanSLC22A46583solute carrier family 22 (organic cation/zwitterion transporter), member 4
img OMIM, Score=1000, UMLKSK CUI: C0016169
HumanSHH6469sonic hedgehog
INFERRED, Score=800, UMLKSK CUI: C0016169
HumanCCL176361chemokine (C-C motif) ligand 17
img GENERIF, Score=694, Pubmed Id: 18004070, UMLKSK CUI: C0016169
HumanSALL16299sal-like 1 (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0016169
HumanPTEN5728phosphatase and tensin homolog
img OMIM, Score=790, UMLKSK CUI: C0016169
HumanPOR5447P450 (cytochrome) oxidoreductase
INFERRED, Score=800, UMLKSK CUI: C0016169
HumanABCB15243ATP-binding cassette, sub-family B (MDR/TAP), member 1
img GENERIF, Score=1000, Pubmed Id: 15505619, UMLKSK CUI: C0016169
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0016169Fistula0self