You are not alone. Here is where to start: learn the basics, find a specialist or center that sees 6q16 deletion syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full 6q16 deletion syndrome hub →6q16 deletion syndrome is a rare condition. Also known as Del(6)(q16), Monosomy 6q16, Prader-Willi-like syndrome due to microdeletion 6q16. Tomeko brings together the specialists, research, clinical trials, treatments and community for 6q16 deletion syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:171829 · ICD-10 Q93.5 · GARD 0020126
Start by learning the basics from an authoritative source, find a specialist or center that sees 6q16 deletion syndrome, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat 6q16 deletion syndrome, filtered to your area.
Tomeko shows live, recruiting studies for 6q16 deletion syndrome from ClinicalTrials.gov on the hub.