Atrioventricular Septal Defect 2 (AVSD2)

Alias:
Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome
Atrioventricular Septal Defect, Susceptibility to, 2
Avsd2
Septal Defect, Atrioventricular, Type 2
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Atrioventricular Septal Defect 2, also known as atrioventricular septal defect, partial, with heterotaxy syndrome, is related to chromosome 3pter-p25 deletion syndrome and heart septal defect. An important gene associated with Atrioventricular Septal Defect 2 is CRELD1 (Cysteine Rich With EGF Like Domains 1). Affiliated tissues include heart and lung, and related phenotypes are atrioventricular canal defect and dextrocardia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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1
8
10

Medical Symptom

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Gene & Mutation

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References Literature

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