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Details
Link-It Detail - Disease - Coronary Artery Disease
Debug Stats
  • ### Total Build Time: 234 ms 54.638 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 344 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 291 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=3 ms Completed: 3 ms rowSize= 986 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 4.041 KB
  • CONCEPT_RELATIONSHIPS gt=183 ms Completed: 183 ms rowSize= 14.883 KB
  • CONCEPT_GENES gt=36 ms Completed: 36 ms rowSize= 32.755 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Coronary Artery Disease C1956346
Definition (1)
Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Coronary Disease C0010068
img Arteriosclerosis C0003850
Ancestral Roots
RootRoot Plus OneDepthParent
img Cardiovascular Diseases C0007222img Heart Diseases C00187995img Coronary Disease C0010068
img Cardiovascular Diseases C0007222img Vascular Diseases C00423735img Coronary Disease C0010068
img Cardiovascular Diseases C0007222img Vascular Diseases C00423735img Arteriosclerosis C0003850
Relationships (356)

Relation Types:
diso_​to_​anat : 33
diso_​to_​chem : 162
diso_​to_​diso : 129
diso_​to_​gene : 2
diso_​to_​phen : 5
diso_​to_​phys : 25


Relationships:
none : 242
associated_​with : 1
isa : 22
location_​of : 1
mapped_​to : 4
may_​prevent : 42
may_​treat : 39
related_​to : 4
used_​for : 1
Page Size
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO2294img Complication Aspects C1171258
DISO_to_ANAT1711img In Blood C0005768
DISO_to_DISO1210img Complication Aspects C1171258
DISO_to_ANAT1132img In Blood C0005768
DISO_to_PHEN1052img genetic aspects C0017399
DISO_to_ANAT902img Coronary Vessel C0010075
DISO_to_DISO728img Calcinosis C0006663
DISO_to_DISO601img Myocardial Infarction C0027051
DISO_to_PHEN531img genetic aspects C0017399
DISO_to_ANAT520img Coronary Vessel C0010075
DISO_to_DISO404img Diabetes Mellitus, Non-Insulin-Dependent C0011860
DISO_to_DISO401img Myocardial Infarction C0027051
DISO_to_CHEM345img Platelet Aggregation Inhibitors C0032177
DISO_to_CHEM309img Sirolimus C0072980
DISO_to_DISO306img Ventricular Dysfunction, Left C0242698
DISO_to_DISO304img Calcinosis C0006663
DISO_to_CHEM286img Hydroxymethylglutaryl-CoA Reductase Inhibitors C0360714
DISO_to_DISO272img Coronary Restenoses C0948480
DISO_to_PHYS266img Coronary Circulation C0010067
DISO_to_CHEM260img Cardiovascular Agents C0007220
DISO_to_DISO255img Myocardial Ischemia C0151744
DISO_to_GENE252img Polymorphism, Single Nucleotide C0752046
DISO_to_DISO243img ACS - Acute coronary syndrome C0948089
DISO_to_PHYS238img Genetic Polymorphism C0032529
DISO_to_DISO236img Atherosclerosis C0004153
Genes (170)

Species:
human : 170
Page Size
Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanCCR2729230chemokine (C-C motif) receptor 2
img GAD, Score=1000, Pubmed Id: 11500196, UMLKSK CUI: C1956346
HumanNCF1C654817neutrophil cytosolic factor 1C pseudogene
img GENERIF, Score=923, Pubmed Id: 16293794, UMLKSK CUI: C1956346
HumanIFNE338376interferon, epsilon
img GENERIF, Score=1000, Pubmed Id: 18362232, UMLKSK CUI: C1956346
HumanUTS2D257313
img GENERIF, Score=1000, Pubmed Id: 16940699, UMLKSK CUI: C1956346
HumanCAQ14171512Circulating adiponectin QTL on chromosome 14
img GENERIF, Score=756, Pubmed Id: 12524229, UMLKSK CUI: C1956346
HumanAPOA5116519apolipoprotein A-V
img GENERIF, Score=1000, Pubmed Id: 18801202, UMLKSK CUI: C1956346
img GENERIF, Score=1000, Pubmed Id: 16258166, UMLKSK CUI: C1956346
img GENERIF, Score=1000, Pubmed Id: 15306190, UMLKSK CUI: C1956346
HumanP2RY1264805purinergic receptor P2Y, G-protein coupled, 12
img GENERIF, Score=1000, Pubmed Id: 16181985, UMLKSK CUI: C1956346
img GENERIF, Score=923, Pubmed Id: 17803810, UMLKSK CUI: C1956346
HumanXYLT264132xylosyltransferase II
img OMIM, Score=1000, UMLKSK CUI: C1956346
HumanXYLT164131xylosyltransferase I
img OMIM, Score=1000, UMLKSK CUI: C1956346
HumanRETN56729resistin
img GENERIF, Score=1000, Pubmed Id: 16822679, UMLKSK CUI: C1956346
img GENERIF, Score=1000, Pubmed Id: 17526982, UMLKSK CUI: C1956346
HumanSLC2A956606solute carrier family 2 (facilitated glucose transporter), member 9
img GENERIF, Score=1000, Pubmed Id: 18398472, UMLKSK CUI: C1956346
HumanAPOM55937apolipoprotein M
img GENERIF, Score=1000, Pubmed Id: 17973931, UMLKSK CUI: C1956346
img GENERIF, Score=1000, Pubmed Id: 17674965, UMLKSK CUI: C1956346
HumanPARL55486presenilin associated, rhomboid-like
img GENERIF, Score=1000, Pubmed Id: 18758826, UMLKSK CUI: C1956346
HumanGHRL51738ghrelin/obestatin prepropeptide
img GENERIF, Score=1000, Pubmed Id: 17884032, UMLKSK CUI: C1956346
HumanADIPOR151094adiponectin receptor 1
img GENERIF, Score=756, Pubmed Id: 17003341, UMLKSK CUI: C1956346
HumanC7orf1610842
img OMIM, Score=743, UMLKSK CUI: C1956346
HumanDHS10774dehydrated hereditary stomatocytosis
img OMIM, Score=1000, UMLKSK CUI: C1956346
HumanKLF210365Kruppel-like factor 2 (lung)
img GENERIF, Score=1000, Pubmed Id: 16617118, UMLKSK CUI: C1956346
HumanLIPG9388lipase, endothelial
img GENERIF, Score=1000, Pubmed Id: 17986713, UMLKSK CUI: C1956346
HumanADIPOQ9370adiponectin, C1Q and collagen domain containing
Click here to display 11 evidence detail records.
HumanPLA2G77941phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma)
img GENERIF, Score=1000, Pubmed Id: 18204052, UMLKSK CUI: C1956346
HumanWRN7486Werner syndrome, RecQ helicase-like
img GENERIF, Score=1000, Pubmed Id: 15246744, UMLKSK CUI: C1956346
HumanVTN7448vitronectin
img GENERIF, Score=1000, Pubmed Id: 12913402, UMLKSK CUI: C1956346
HumanVEGFA7422vascular endothelial growth factor A
img GENERIF, Score=1000, Pubmed Id: 15754021, UMLKSK CUI: C1956346
HumanVCAM17412vascular cell adhesion molecule 1
img GENERIF, Score=756, Pubmed Id: 12940514, UMLKSK CUI: C1956346
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1956346Coronary Artery Disease0self