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Details
Link-It Detail - Disease - Aortic Diseases
Debug Stats
  • ### Total Build Time: 97 ms 37.104 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 384 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 314 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=21 ms Completed: 21 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= 553 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 1.810 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.505 KB
  • CONCEPT_RELATIONSHIPS gt=24 ms Completed: 24 ms rowSize= 13.822 KB
  • CONCEPT_GENES gt=41 ms Completed: 41 ms rowSize= 17.385 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.149 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Aortic Diseases C0003493
3-83 DISEASES OF THE AORTA
Definition (1)
condition in which there is a deviation from or interruption of the normal structure or function of the aorta, which is the main trunk of the systemic arteries.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Vascular Diseases C0042373
Children (4)
img Aortic Aneurysm C0003486
img Aortitis C0003509
img Leriche Syndrome C0023370
img Aortic Arch Syndromes C0003490
Ancestral Roots
RootRoot Plus OneDepthParent
img Cardiovascular Diseases C0007222img Vascular Diseases C00423733img Vascular Diseases C0042373
Relationships (139)

Relation Types:
diso_​to_​anat : 22
diso_​to_​chem : 5
diso_​to_​diso : 109
diso_​to_​phen : 2
diso_​to_​phys : 1


Relationships:
none : 114
associated_​with : 1
entry_​version_​of : 1
isa : 21
location_​of : 1
mapped_​to : 1
Page Size
Current 25
  Page 1 of 6
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT551img Aorta, Thoracic C1522460
DISO_to_DISO395img Complication Aspects C1171258
DISO_to_DISO345img Atherosclerosis C0004153
DISO_to_DISO303img Complication Aspects C1171258
DISO_to_DISO212img Fistula, Vascular C0080304
DISO_to_DISO204img Arteriosclerosis C0003850
DISO_to_DISO203img Calcinosis C0006663
DISO_to_ANAT196img Aorta, Thoracic C1522460
DISO_to_ANAT173img Aorta C0003483
DISO_to_ANAT154img Abdominal aorta structure C0003484
DISO_to_DISO146img Fistula, Vascular C0080304
DISO_to_PHEN126img genetic aspects C0017399
DISO_to_DISO118img ARTERIAL OBSTRUCTIVE DIS C0003838
DISO_to_DISO114img Calcinosis C0006663
DISO_to_DISO113img Thrombosis C0040053
DISO_to_DISO103img Intestinal Fistula C0021833
DISO_to_ANAT96img Abdominal aorta structure C0003484
DISO_to_ANAT90img Aorta C0003483
DISO_to_DISO87img ARTERIAL OBSTRUCTIVE DIS C0003838
DISO_to_DISO83img Intestinal Fistula C0021833
DISO_to_ANAT78img In Blood C0005768
DISO_to_ANAT74img Aortic Valve C0003501
DISO_to_DISO73img Coronary Artery Disease C1956346
DISO_to_DISO70img Hematoma C0018944
DISO_to_DISO70img Ulcer C0041582
Genes (60)

Species:
human : 60
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanSLC2A1081031solute carrier family 2 (facilitated glucose transporter), member 10
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanXYLT164131xylosyltransferase I
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanRTN457142reticulon 4
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanRETN56729resistin
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanEFEMP230008EGF containing fibulin-like extracellular matrix protein 2
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanHPSE10855heparanase
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanFBLN510516fibulin 5
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanADIPOQ9370adiponectin, C1Q and collagen domain containing
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanTNFSF98744tumor necrosis factor (ligand) superfamily, member 9
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanPLA2G77941phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma)
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanTIMP37078TIMP metallopeptidase inhibitor 3
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanTIMP27077TIMP metallopeptidase inhibitor 2
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanTIMP17076TIMP metallopeptidase inhibitor 1
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanTGFBR27048transforming growth factor, beta receptor II (70/80kDa)
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanTGFBR17046transforming growth factor, beta receptor 1
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanTGFB17040transforming growth factor, beta 1
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanTRG@6965
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanTRD@6964
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanCX3CL16376chemokine (C-X3-C motif) ligand 1
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanPROC5624protein C (inactivator of coagulation factors Va and VIIIa)
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanPRKCB5579protein kinase C, beta
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanSERPINE15054serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanNOTCH14851notch 1
INFERRED, Score=800, UMLKSK CUI: C0003493
HumanNOS34846nitric oxide synthase 3 (endothelial cell)
INFERRED, Score=800, UMLKSK CUI: C0003493
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0003493Aortic Diseases0self