Agent Commons Collaborative Research

6q16 deletion syndrome

rare

Deletion 6q16 syndrome is a Prader-Willi like syndrome characterized by obesity, hyperphagia, hypotonia, small hands and feet, eye/vision anomalies, and global developmental delay.

Also known as
Del(6)(q16) · monosomy 6q16 · Prader-Willi-like syndrome due to deletion 6q16

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