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Details
Link-It Detail - Disease - Coronary Disease
Debug Stats
  • ### Total Build Time: 148 ms 53.179 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 330 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 423 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=5 ms Completed: 5 ms rowSize= 555 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 2.678 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 2.776 KB
  • CONCEPT_RELATIONSHIPS gt=88 ms Completed: 88 ms rowSize= 14.472 KB
  • CONCEPT_GENES gt=39 ms Completed: 39 ms rowSize= 30.614 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Coronary Disease C0010068
Definition (1)
An imbalance between myocardial functional requirements and the capacity of the CORONARY VESSELS to supply sufficient blood flow. It is a form of MYOCARDIAL ISCHEMIA (insufficient blood supply to the heart muscle) caused by a decreased capacity of the coronary vessels.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Myocardial Ischemia C0151744
Children (6)
img Coronary Occlusion C0151814
img Coronary Aneurysm C0010051
img Coronary Vasospasm C0010073
img Coronary Thrombosis C0010072
img Coronary Stenosis C0242231
img Coronary Artery Disease C1956346
Ancestral Roots
RootRoot Plus OneDepthParent
img Cardiovascular Diseases C0007222img Heart Diseases C00187994img Myocardial Ischemia C0151744
img Cardiovascular Diseases C0007222img Vascular Diseases C00423734img Myocardial Ischemia C0151744
Relationships (240)

Relation Types:
diso_​to_​anat : 21
diso_​to_​chem : 113
diso_​to_​diso : 83
diso_​to_​gene : 4
diso_​to_​phen : 2
diso_​to_​phys : 17


Relationships:
none : 195
gene_​associated_​with_​disease : 2
is_​associated_​anatomic_​site_​of : 4
may_​prevent : 3
may_​treat : 33
permuted_​term_​of : 1
use : 2
Page Size
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT1423img In Blood C0005768
DISO_to_DISO1040img Complication Aspects C1171258
DISO_to_ANAT1014img In Blood C0005768
DISO_to_DISO701img Complication Aspects C1171258
DISO_to_PHEN487img genetic aspects C0017399
DISO_to_PHEN485img genetic aspects C0017399
DISO_to_DISO475img Myocardial Infarction C0027051
DISO_to_CHEM332img Hydroxymethylglutaryl-CoA Reductase Inhibitors C0360714
DISO_to_DISO313img Myocardial Infarction C0027051
DISO_to_CHEM272img Hydroxymethylglutaryl-CoA Reductase Inhibitors C0360714
DISO_to_DISO267img Diabetes Mellitus, Non-Insulin-Dependent C0011860
DISO_to_CHEM257img Platelet Aggregation Inhibitors C0032177
DISO_to_ANAT253img Coronary Vessel C0010075
DISO_to_DISO237img Diabetes Mellitus, Non-Insulin-Dependent C0011860
DISO_to_DISO223img Cerebrovascular accident C0038454
DISO_to_DISO222img Hypertension C0020538
DISO_to_CHEM207img Agents, Anticholesteremic C0003277
DISO_to_DISO207img Angiopathies, Diabetic C0011875
DISO_to_DISO188img Calcinosis C0006663
DISO_to_CHEM186img C-Reactive Protein C0006560
DISO_to_DISO184img Cerebrovascular accident C0038454
DISO_to_PHYS181img Coronary Circulation C0010067
DISO_to_CHEM175img Cholesterol, LDL C0023824
DISO_to_PHYS163img Genetic Polymorphism C0032529
DISO_to_DISO155img Hyperlipidemia C0020473
Genes (231)

Species:
human : 231
Page Size
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SpeciesGeneGeneIdGene NameEvidence
HumanCCR2729230chemokine (C-C motif) receptor 2
img GAD, Score=1000, Pubmed Id: 11500196, UMLKSK CUI: C0010068
HumanNCF1C654817neutrophil cytosolic factor 1C pseudogene
img GENERIF, Score=923, Pubmed Id: 16293794, UMLKSK CUI: C0010068
HumanIFNE338376interferon, epsilon
img GENERIF, Score=1000, Pubmed Id: 18362232, UMLKSK CUI: C0010068
HumanUTS2D257313
img GENERIF, Score=1000, Pubmed Id: 16940699, UMLKSK CUI: C0010068
HumanPCSK9255738proprotein convertase subtilisin/kexin type 9
img GENERIF, Score=1000, Pubmed Id: 16554528, UMLKSK CUI: C0010068
HumanKIF6221458kinesin family member 6
img GENERIF, Score=1000, Pubmed Id: 18510970, UMLKSK CUI: C0010068
HumanCAQ14171512Circulating adiponectin QTL on chromosome 14
img GENERIF, Score=756, Pubmed Id: 12524229, UMLKSK CUI: C0010068
HumanAPOA5116519apolipoprotein A-V
Click here to display 5 evidence detail records.
HumanCNDP184735carnosine dipeptidase 1 (metallopeptidase M20 family)
img GENERIF, Score=1000, Pubmed Id: 16965804, UMLKSK CUI: C0010068
HumanVKORC179001vitamin K epoxide reductase complex, subunit 1
img GENERIF, Score=835, Pubmed Id: 17549303, UMLKSK CUI: C0010068
HumanP2RY1264805purinergic receptor P2Y, G-protein coupled, 12
img GENERIF, Score=923, Pubmed Id: 17803810, UMLKSK CUI: C0010068
img GENERIF, Score=1000, Pubmed Id: 16181985, UMLKSK CUI: C0010068
HumanXYLT264132xylosyltransferase II
INFERRED, Score=800, UMLKSK CUI: C0010068
HumanXYLT164131xylosyltransferase I
INFERRED, Score=800, UMLKSK CUI: C0010068
HumanRETN56729resistin
img GENERIF, Score=1000, Pubmed Id: 16822679, UMLKSK CUI: C0010068
img GENERIF, Score=1000, Pubmed Id: 17526982, UMLKSK CUI: C0010068
HumanSLC2A956606solute carrier family 2 (facilitated glucose transporter), member 9
img GENERIF, Score=1000, Pubmed Id: 18398472, UMLKSK CUI: C0010068
HumanAPOM55937apolipoprotein M
img GENERIF, Score=1000, Pubmed Id: 17674965, UMLKSK CUI: C0010068
img GENERIF, Score=1000, Pubmed Id: 17973931, UMLKSK CUI: C0010068
HumanPARL55486presenilin associated, rhomboid-like
img GENERIF, Score=1000, Pubmed Id: 18758826, UMLKSK CUI: C0010068
HumanUGT1A154658UDP glucuronosyltransferase 1 family, polypeptide A1
img GENERIF, Score=1000, Pubmed Id: 17952380, UMLKSK CUI: C0010068
HumanGHRL51738ghrelin/obestatin prepropeptide
img GENERIF, Score=1000, Pubmed Id: 17884032, UMLKSK CUI: C0010068
HumanGP651206glycoprotein VI (platelet)
img GENERIF, Score=1000, Pubmed Id: 17105818, UMLKSK CUI: C0010068
HumanINSIG251141insulin induced gene 2
img GENERIF, Score=1000, Pubmed Id: 18989534, UMLKSK CUI: C0010068
HumanADIPOR151094adiponectin receptor 1
img GENERIF, Score=756, Pubmed Id: 17003341, UMLKSK CUI: C0010068
HumanBHMT223743betaine--homocysteine S-methyltransferase 2
img GENERIF, Score=1000, Pubmed Id: 12818402, UMLKSK CUI: C0010068
HumanC7orf1610842
INFERRED, Score=800, UMLKSK CUI: C0010068
HumanDHS10774dehydrated hereditary stomatocytosis
INFERRED, Score=800, UMLKSK CUI: C0010068
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0010068Coronary Disease0self