Congenital Heart Defects, Multiple Types, 2 (CHTD2)

Alias:
Chtd2
Heart Defects, Congenital, Nonsyndromic, Type 2 (chtd2
Congenital Heart Defects, Nonsyndromic, 2
Congenital Heart Defects Non-Syndromic 2
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Heart Defects, Multiple Types, 2, also known as chtd2, is related to pelvic organ prolapse and atrial septal defect 2. An important gene associated with Congenital Heart Defects, Multiple Types, 2 is TAB2 (TGF-Beta Activated Kinase 1 (MAP3K7) Binding Protein 2). Affiliated tissues include heart and skin, and related phenotypes are aortic regurgitation and congestive heart failure
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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
4
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Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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