Sudden Cardiac Failure, Infantile; Scfi
Clinical Features
Top most frequent phenotypes and symptoms related to Sudden Cardiac Failure, Infantile; Scfi
- Seizures
- Generalized hypotonia
- Failure to thrive
- Feeding difficulties
- Cardiomyopathy
- Myopathy
- Vomiting
- Congestive heart failure
- Arrhythmia
- Acidosis
And another 10 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Sudden Cardiac Failure, Infantile; Scfi Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
PPA2.
By Fulgent Genetics Fulgent Genetics (United States).
PPA2
Specificity
100 %
Genes
100 % |
Cardiomyopathy Panel.
By Blueprint Genetics (Finland).
RIT1, RRAS, RYR2, SCN5A, SCNN1B, SCNN1G, SCO2, SDHA, SGCA, SGCB, SGCD, SGCG, SLC22A5, BRAF, SLC25A4, SOS1, SOS2, TAZ, TBX20, TBX5 , (...)
View the complete list with 133 more genes
Specificity
1 %
Genes
100 % |
Arrhythmia Panel.
By Blueprint Genetics (Finland).
RYR2, SCN10A, SCN1B, SCN5A, TBX5, TGFB3, TNNI3, TNNT2, TRDN, TTN, CACNA1C, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, LDB3, SALL4, NOS1AP , (...)
View the complete list with 35 more genes
Specificity
2 %
Genes
100 % |
Comprehensive Cardiology Panel.
By Blueprint Genetics (Finland).
RIT1, RRAS, RYR2, SCN10A, SCN1B, SCN5A, SCNN1B, SCNN1G, SCO2, SDHA, SGCA, SGCB, SGCD, SGCG, SLC22A5, BRAF, SLC25A4, SOS1, SOS2, TAZ , (...)
View the complete list with 163 more genes
Specificity
1 %
Genes
100 % |
You can get up to -4 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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