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618497.1
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Subject Details
Country
Saudi Arabia
HPO Terms
Delayed speech and language development; Specific learning disability; Motor delay; Failure to thrive
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Sex
Female
Family History
Yes
Parental Consanguinity
No
Subject Variants
Variant Name
Allele Count
Associated Disease
NM_000718.4:c.6377G>A
1
Neurodevelopmental Disorder with Seizures and Nonepileptic Hyperkinetic Movements
NM_000718.4:c.6935A>G
1
Neurodevelopmental Disorder with Seizures and Nonepileptic Hyperkinetic Movements
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References
Monies et al. 2017
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العربية
About Us
News
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العربية
Home
About Us
CTGA Database
CTGA Overview
Search Database
Submit to Database
Publications
Research Articles
Genetics Made Easy
Genetic Disorders in the Arab World
Reports
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News
Gallery
Fellowships
Contact Us