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Results 1 - 10 of 157 for Heart block
  1. TRPM4 gene 
    ... gene have been found to cause progressive familial heart block. This condition alters the normal beating of the ... coordinate normal heartbeats. Interruption of this signaling causes heart block. Death of these impaired cardiac cells over time ...
    https://medlineplus.gov/genetics/gene/trpm4 - Genetics
  2. SCN10A gene 
    ... associated with a type of arrhythmia known as heart block. Heart block occurs when the heart's electrical signals are ... to the NaV1.8 sodium channel lead to heart block. hPN3 Nav1.8 peripheral nerve sodium channel 3 ...
    https://medlineplus.gov/genetics/gene/scn10a - Genetics
  3. SCN5A gene 
    ... gene have been found to cause progressive familial heart block. This condition alters the normal beating of the ... heartbeats. Interruption of this signaling is known as heart block. The impaired cardiac cells die, leading to a ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  4. ADAMTS13 gene 
    ... speech), fever, abnormal kidney function, abdominal pain, and heart problems.Most of these mutations change single protein building blocks (amino acids) in the ADAMTS13 enzyme. Other mutations ...
    https://medlineplus.gov/genetics/gene/adamts13 - Genetics
  5. KANK2 gene 
    ... hair, type IV does not appear to cause heart disease.The identified mutation changes a single protein building block (amino acid) in SIP, replacing the amino acid ...
    https://medlineplus.gov/genetics/gene/kank2 - Genetics
  6. TNNI3 gene 
    ... troponin I helps to coordinate contraction of the heart. When calcium levels are low, the troponin complex binds to the thin filament. This binding blocks the interaction between the thick and thin filaments ...
    https://medlineplus.gov/genetics/gene/tnni3 - Genetics
  7. ABCC9 gene 
    ... hair growth (hypertrichosis), a distinctive facial appearance, and heart defects. Each of the mutations changes a single protein building block (amino acid) in the SUR2 protein. These changes ...
    https://medlineplus.gov/genetics/gene/abcc9 - Genetics
  8. TNNT2 gene 
    ... all affected individuals have an increased risk of heart failure and sudden death.Most TNNT2 gene mutations in familial hypertrophic cardiomyopathy change single protein building blocks (amino acids) in the cardiac troponin T protein. ...
    https://medlineplus.gov/genetics/gene/tnnt2 - Genetics
  9. APOB gene 
    ... the blood and an increased risk of developing heart disease. Each mutation that causes this condition changes a single protein building block (amino acid) in a critical region of apolipoprotein ...
    https://medlineplus.gov/genetics/gene/apob - Genetics
  10. MT-TE gene 
    ... muscle weakness (myopathy) and problems with their eyes, heart, or kidneys. The mutation involved in this condition replaces the DNA building block (nucleotide) thymine with the nucleotide cytosine at position ...
    https://medlineplus.gov/genetics/gene/mt-te - Genetics
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