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Details
Link-It Detail - Disease - Cardiovascular Diseases
Debug Stats
  • ### Total Build Time: 232 ms 38.053 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= 273 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=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 2.280 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=149 ms Completed: 149 ms rowSize= 14.861 KB
  • CONCEPT_GENES gt=74 ms Completed: 74 ms rowSize= 18.919 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Cardiovascular Diseases C0007222
Definition (1)
Pathological conditions involving the CARDIOVASCULAR SYSTEM including the HEART; the BLOOD VESSELS; or the PERICARDIUM.
Semantic Types (1)
Disease or Syndrome (T047)
Children (5)
img Heart Diseases C0018799
img Vascular Diseases C0042373
img Cardiovascular Infections C0596270
img Cardiovascular Abnormalities C0243050
img Pregnancy Complications, Cardiovascular C0032963
Relationships (389)

Relation Types:
diso_​to_​anat : 30
diso_​to_​chem : 146
diso_​to_​diso : 174
diso_​to_​gene : 2
diso_​to_​phen : 5
diso_​to_​phys : 32


Relationships:
none : 313
associated_​with : 2
classifies : 1
gene_​is_​biomarker_​of : 1
isa : 26
location_​of : 1
mapped_​to : 14
may_​diagnose : 22
may_​treat : 9
Page Size
Current 25
  Page 1 of 16
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT2655img In Blood C0005768
DISO_to_DISO1440img Complication Aspects C1171258
DISO_to_DISO1413img Diabetes Mellitus, Type 2 C0011860
DISO_to_ANAT1280img In Blood C0005768
DISO_to_PHEN1232img genetic aspects C0017399
DISO_to_DISO968img Obesity C0028754
DISO_to_DISO955img Hypertension C0020538
DISO_to_DISO921img Metabolic Syndrome X C0524620
DISO_to_DISO854img chemically induced C0007994
DISO_to_CHEM730img Hydroxymethylglutaryl-CoA Reductase Inhibitors C0360714
DISO_to_DISO730img Complication Aspects C1171258
DISO_to_DISO708img Hypertension C0020538
DISO_to_DISO675img Diabetes Mellitus, Non-Insulin-Dependent C0011860
DISO_to_PHEN653img genetic aspects C0017399
DISO_to_DISO597img Kidney Failure, Chronic C0022661
DISO_to_DISO526img Obesity C0028754
DISO_to_DISO524img Diabetes Mellitus C0011849
DISO_to_DISO522img chemically induced C0007994
DISO_to_DISO509img Kidney Diseases C0022658
DISO_to_PHYS462img Blood Pressure C0005823
DISO_to_DISO440img Neoplasms C0027651
DISO_to_DISO426img Kidney Failure, Chronic C0022661
DISO_to_ANAT391img Endothelium, Vascular C0014261
DISO_to_DISO380img Metabolic Syndrome X C0524620
DISO_to_CHEM377img C-Reactive Protein C0006560
Genes (1652)

Species:
human : 1652
Page Size
Current 25
  Page 1 of 67
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLOC100507436100507436
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanCD24100133941CD24 molecule
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanSPANXB1728695SPANX family, member B1
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanCSAG2728461CSAG family, member 2
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanGGT2728441gamma-glutamyltransferase 2
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanD2HGDH728294D-2-hydroxyglutarate dehydrogenase
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanPPBPL1728045
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanNCF1C654817neutrophil cytosolic factor 1C pseudogene
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanOR13G1441933olfactory receptor, family 13, subfamily G, member 1
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanMIAT440823myocardial infarction associated transcript (non-protein coding)
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanSLEB4404714systemic lupus erythematosus, susceptibility to, 4
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanSLC25A5P8392301solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 5 pseudogene 8
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanLOC391533391533
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanSUMO4387082small ubiquitin-like modifier 4
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanTRIM74378108tripartite motif containing 74
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanSLC6A18348932solute carrier family 6 (neutral amino acid transporter), member 18
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanSLC6A19340024solute carrier family 6 (neutral amino acid transporter), member 19
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanFAM5C339479family with sequence similarity 5, member C
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanIFNE338376interferon, epsilon
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanSERPINA9327657serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 9
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanCYP4V2285440cytochrome P450, family 4, subfamily V, polypeptide 2
INFERRED, Score=800, UMLKSK CUI: C0007222
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
INFERRED, Score=800, UMLKSK CUI: C0007222
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0007222Cardiovascular Diseases0self