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216550.7
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Subject Details
Country
Lebanon
HPO Terms
Hypotonia; Obesity; Short stature; Global developmental delay
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Sex
Unknown
Parental Consanguinity
No
Subject Variants
Variant Name
Allele Count
Associated Disease
NM_017890.4:c.11785C>G
2
Cohen Syndrome
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References
Jalkh et al. 2019
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العربية
About Us
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Fellowships
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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