6q16 deletion syndrome

MONDO:0015749

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), Prader-Willi-like syndrome due to deletion 6q16, monosomy 6q16

0 clinical trials for this condition and its sub-types, 0 tagged with 6q16 deletion syndrome itself.

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↑ Prader-Willi-like syndrome (0) ↑ Partial deletion of the long arm of chromosome 6 (0)

Including sub-types (0) Tagged with 6q16 deletion syndrome (0)

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