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613690.1
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Subject Details
Country
Lebanon
HPO Terms
Hypertrophic cardiomyopathy;
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Sex
Female
Family History
Yes
Parental Consanguinity
No
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_000363.5:c.61C>T
1
Cardiomyopathy, Familial Hypertrophic 7
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Remarks
Similarly affected father and 2 siblings
References
Fahed et al. 2020
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