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Browse result for Progressive familial heart block

※ introduction

    A heart conduction disease characterized by autosomal dominant inheritance of a cardiac conduction defect that may progress to complete atrioventricular (AV) block and maybe asymptomatic of manifest as shortness of breath, dizziness, syncope, abdominal pain, heart failure or sudden death.

Reference
DiseaseOntology: Progressive familial heart block



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD01751Q145246331
SCN5A
Sodium channel protein type 5 subunit alpha
Homo sapiens
PTMD10363Q8TD4354795
TRPM4
Transient receptor potential cation channel subfamily M member 4
Homo sapiens