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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
Reference
DiseaseOntology: Progressive familial heart block
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD01751 | Q14524 | 6331 | SCN5A | Sodium channel protein type 5 subunit alpha | Homo sapiens |
| PTMD10363 | Q8TD43 | 54795 | TRPM4 | Transient receptor potential cation channel subfamily M member 4 | Homo sapiens |
