Ventricular Septal Defect

Alias:
Ventricular Septal Defects
Interventricular Septal Defect
Congenital Ventricular Septal Defect
Heart Septal Defects, Ventricular
Vsd - [ventricular Septum Defect]
Single Ventricular Septal Defect
Ventricular Septal Abnormality
Interventricular Septum Defect
Septal, Ventricular Defect
Ventricular Septum Defect
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Ventricular Septal Defect, also known as interventricular septal defect, is related to tetralogy of fallot and double outlet right ventricle. An important gene associated with Ventricular Septal Defect is FOXP4 (Forkhead Box P4), and among its related pathways/superpathways are Nervous system development and Human Embryonic Stem Cell Pluripotency. The drugs Salbutamol and Ropivacaine have been mentioned in the context of this disorder. Affiliated tissues include heart and lung, and related phenotypes are Increased shRNA abundance (Z-score > 2) and muscle
Related ID:
MESH:D006345
ICD11:668140715

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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75
879
1

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
No Data Found!
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