Progressive Familial Heart Block (HBBD)

Alias:
Hereditary Bundle Branch System Defect
Progressive Cardiac Conduction Defect
Hereditary Bundle Branch Defect
Heart Block Progressive, Familial
Familial Progressive Heart Block
Familial Lev-Lenegre Disease
Familial Lenegre Disease
Familial Lev Disease
Bundle Branch Block
Lenegre Lev Disease
Lev-Lenègre Disease
Bundle-Branch Block
Familial Pccd
Lev's Disease
Lev Syndrome
Pccd
Hbbd
Pfhb
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Progressive Familial Heart Block, also known as hereditary bundle branch system defect, is related to progressive familial heart block, type ia and left bundle branch hemiblock, and has symptoms including dyspnea and syncopal episode. An important gene associated with Progressive Familial Heart Block is TRPM4 (Transient Receptor Potential Cation Channel Subfamily M Member 4), and among its related pathways/superpathways are Cardiac conduction and Neuroscience. The drugs Prednisolone and Prednisolone acetate have been mentioned in the context of this disorder. Affiliated tissues include heart and atrioventricular node, and related phenotypes are Decreased shRNA abundance and muscle
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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15
138
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Medical Symptom

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Gene & Mutation

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MGI
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References Literature

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