You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Paternal 14q32.2 microdeletion syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full Paternal 14q32.2 microdeletion syndrome hub →Paternal 14q32.2 microdeletion syndrome is a rare condition. Also known as Paternal del(14)(q32.2). Tomeko brings together the specialists, research, clinical trials, treatments and community for Paternal 14q32.2 microdeletion syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:254525 · OMIM 616222 · ICD-10 Q93.5 · GARD 0017220
Start by learning the basics from an authoritative source, find a specialist or center that sees Paternal 14q32.2 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 Paternal 14q32.2 microdeletion syndrome, filtered to your area.
Tomeko shows live, recruiting studies for Paternal 14q32.2 microdeletion syndrome from ClinicalTrials.gov on the hub.