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Details
Link-It Detail - Disease - Foramen Ovale, Patent
Debug Stats
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  • Reload Stats
Disease (1)
Foramen Ovale, Patent C0016522
Definition (1)
A condition in which the FORAMEN OVALE in the ATRIAL SEPTUM fails to close shortly after birth. This results in abnormal communications between the two upper chambers of the heart. An isolated patent ovale foramen without other structural heart defects is usually of no hemodynamic significance.
Semantic Types (2)
Congenital Abnormality (T019)
Disease or Syndrome (T047)
Parents (1)
img Heart Septal Defects, Atrial C0018817
Ancestral Roots
RootRoot Plus OneDepthParent
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007687img Heart Septal Defects, Atrial C0018817
img Cardiovascular Diseases C0007222img Cardiovascular Abnormalities C02430506img Heart Septal Defects, Atrial C0018817
img Cardiovascular Diseases C0007222img Heart Diseases C00187996img Heart Septal Defects, Atrial C0018817
Relationships (28)

Relation Types:
diso_​to_​anat : 6
diso_​to_​diso : 22


Relationships:
none : 21
clinically_​similar : 1
is_​associated_​anatomic_​site_​of : 4
permuted_​term_​of : 1
used_​for : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO514img Complication Aspects C1171258
DISO_to_DISO183img Cerebrovascular accident C0038454
DISO_to_DISO136img Crossed Embolism C0238096
DISO_to_DISO71img Migraine Disorders C0149931
DISO_to_DISO68img Pulmonary Embolism C0034065
DISO_to_DISO60img Atrial Septal Defects C0018817
DISO_to_DISO55img Thrombosis C0040053
DISO_to_DISO44img Anoxia C0003130
DISO_to_DISO38img Migraine with Aura C0154723
DISO_to_DISO34img Brain Ischemia C0007786
DISO_to_DISO34img Ischemic Attack, Transient C0007787
DISO_to_DISO28img Dyspnea C0013404
DISO_to_DISO27img Embolism, Intracranial C0752140
DISO_to_DISO22img Heart Diseases C0018799
DISO_to_DISO21img Heart Aneurysm C0018789
DISO_to_ANAT18img Heart Atria C0018792
DISO_to_DISO18img Atrial Fibrillation C0004238
DISO_to_ANAT17img Atrial Septum C0225836
DISO_to_DISO17img COMPL POSTOP C0032787
DISO_to_DISO17img Venous Thrombosis C0042487
DISO_to_DISO16img Embolism C0013922
DISO_to_ANATis_associated_anatomic_site_ofimg Cardiovascular System C0007226
DISO_to_ANATis_associated_anatomic_site_ofimg Chest C0817096
DISO_to_ANATis_associated_anatomic_site_ofimg Heart C0018787
DISO_to_ANATis_associated_anatomic_site_ofimg Respiratory System C0035237
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanTSFM10102Ts translation elongation factor, mitochondrial
img OMIM, Score=1000, UMLKSK CUI: C0016522
HumanNF14763neurofibromin 1
img OMIM, Score=1000, UMLKSK CUI: C0016522
HumanF52153coagulation factor V (proaccelerin, labile factor)
img GENERIF, Score=1000, Pubmed Id: 17525392, UMLKSK CUI: C0016522
img GENERIF, Score=1000, Pubmed Id: 12695749, UMLKSK CUI: C0016522
HumanF22147coagulation factor II (thrombin)
img GENERIF, Score=1000, Pubmed Id: 17525392, UMLKSK CUI: C0016522
img GENERIF, Score=1000, Pubmed Id: 12695749, UMLKSK CUI: C0016522
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0016522Foramen Ovale, Patent0self