Patent Foramen Ovale

Alias:
Atrial Septal Defect, Ostium Secundum Type
Atrial Septal Defect Within Oval Fossa
Asd, Ostium Secundum Type
Foramen Ovale, Patent
Foramen Ovale Patent
Defect, Patent or Persistent, Ostium Secundum
Ostium Secundum Type Atrial Septal Defect
Ostium Secundum Atrial Septal Defect
Secundum Atrial Septal Defect
Pfo - [patent Foramen Ovale]
Persistent Ostium Secundum
Persistent Foramen Ovale
Open Foramen Ovale
Open Oval Foramen
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Patent Foramen Ovale, also known as atrial septal defect, ostium secundum type, is related to tricuspid atresia and hypoplastic right heart syndrome. An important gene associated with Patent Foramen Ovale is TBX5 (T-Box Transcription Factor 5), and among its related pathways/superpathways are Cardiac conduction and MAPK signaling pathway. The drugs Warfarin and Rivaroxaban have been mentioned in the context of this disorder. Affiliated tissues include heart and brain, and related phenotypes are left-to-right shunt and fatigue
Related ID:
MESH:D054092
ICD11:1618980674

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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106
1123
1

Medical Symptom

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Gene & Mutation

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Related Drugs

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MGI
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References Literature

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