You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Proximal 16p11.2 microdeletion syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full Proximal 16p11.2 microdeletion syndrome hub →Proximal 16p11.2 microdeletion syndrome is a rare condition. Also known as Proximal del(16)(p11.2), Proximal monosomy 16p11.2. Tomeko brings together the specialists, research, clinical trials, treatments and community for Proximal 16p11.2 microdeletion syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:261197 · OMIM 611913 · ICD-10 Q93.5 · GARD 0010740
Start by learning the basics from an authoritative source, find a specialist or center that sees Proximal 16p11.2 microdeletion 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 Proximal 16p11.2 microdeletion syndrome, filtered to your area.
Tomeko shows live, recruiting studies for Proximal 16p11.2 microdeletion syndrome from ClinicalTrials.gov on the hub.