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Details
Link-It Detail - Disease - Aortic Coarctation
Debug Stats
  • ### Total Build Time: 52 ms 24.078 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 306 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= 191 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 561 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.124 KB
  • CONCEPT_RELATIONSHIPS gt=32 ms Completed: 32 ms rowSize= 13.605 KB
  • CONCEPT_GENES gt=4 ms Completed: 4 ms rowSize= 3.802 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Aortic Coarctation C0003492
Definition (1)
Congenital narrowing of a segment of the aorta. Signs and symptoms include hypertension, muscle weakness, shortness of breath, headaches and leg cramps.
Semantic Types (1)
Congenital Abnormality (T019)
Parents (1)
img Heart Defects, Congenital C0018798
Ancestral Roots
RootRoot Plus OneDepthParent
img Cardiovascular Diseases C0007222img Heart Diseases C00187994img Heart Defects, Congenital C0018798
img Cardiovascular Diseases C0007222img Cardiovascular Abnormalities C02430504img Heart Defects, Congenital C0018798
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007685img Heart Defects, Congenital C0018798
Relationships (76)

Relation Types:
diso_​to_​anat : 13
diso_​to_​chem : 15
diso_​to_​diso : 46
diso_​to_​phen : 1
diso_​to_​phys : 1


Relationships:
none : 40
associated_​with : 1
classifies : 1
location_​of : 1
mapped_​to : 17
may_​treat : 15
use : 1
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO238img Complication Aspects C1171258
DISO_to_DISO198img Complication Aspects C1171258
DISO_to_ANAT135img Aorta, Thoracic C1522460
DISO_to_ANAT80img Aorta, Thoracic C1522460
DISO_to_DISO65img Hypertension C0020538
DISO_to_DISO56img Aortic Aneurysm, Thoracic C0162872
DISO_to_DISO53img Aortic Aneurysm C0003486
DISO_to_DISO52img Hypertension C0020538
DISO_to_DISO51img COMPL POSTOP C0032787
DISO_to_ANAT41img Aorta C0003483
DISO_to_DISO38img Abnormalities, Multiple C0000772
DISO_to_ANAT35img Aorta C0003483
DISO_to_DISO32img Aortic Aneurysm C0003486
DISO_to_DISO28img COMPL POSTOP C0032787
DISO_to_DISO27img Aneurysm, False C1510412
DISO_to_DISO26img Aortic Aneurysm, Thoracic C0162872
DISO_to_ANAT25img Abdominal aorta structure C0003484
DISO_to_ANAT24img Structure of subclavian artery C0038530
DISO_to_ANAT23img Aortic Valve C0003501
DISO_to_DISO22img Heart Septal Defects, Ventricular C0018818
DISO_to_DISO21img Aortic Valve Stenosis C0003507
DISO_to_DISO19img ANEURYSM, DISSECTING C0002949
DISO_to_DISO19img Heart Defects, Congenital C0018798
DISO_to_PHYS19img Blood Pressure C0005823
DISO_to_DISO18img Abnormalities, Multiple C0000772
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanSTRA664220stimulated by retinoic acid 6
img OMIM, Score=1000, UMLKSK CUI: C0003492
HumanMKS154903Meckel syndrome, type 1
img OMIM, Score=1000, UMLKSK CUI: C0003492
HumanDHCR717177-dehydrocholesterol reductase
img OMIM, Score=1000, UMLKSK CUI: C0003492
HumanJAG1182jagged 1
img OMIM, Score=1000, UMLKSK CUI: C0003492
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0003492Aortic Coarctation0self