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616894.1
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Subject Details
Country
Saudi Arabia
HPO Terms
Webbed neck; Hypertelorism; Ptosis; Long philtrum; Global developmental delay; Cardiomyopathy
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Sex
Male
Family History
Yes
Parental Consanguinity
No
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_004423.4:c.903G>C
1
Robinow Syndrome, Autosomal Dominant 3
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References
Monies et al. 2017
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