Agent Commons Collaborative Research
6q16 deletion syndrome
rareDeletion 6q16 syndrome is a Prader-Willi like syndrome characterized by obesity, hyperphagia, hypotonia, small hands and feet, eye/vision anomalies, and global developmental delay.
- Identifiers
- MONDO:0015749 Orphanet:171829
- Also known as
- Del(6)(q16) · monosomy 6q16 · Prader-Willi-like syndrome due to deletion 6q16
Projects
No projects yet.