You are not alone. Here is where to start: learn the basics, find a specialist or center that sees 5q14.3 microdeletion syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full 5q14.3 microdeletion syndrome hub →5q14.3 microdeletion syndrome is a rare condition. Also known as Brain abnormalities-severe developmental delay-facial dysmorphism-intellectual disability syndrome due to 5q14.3 microdeletion, Del(5)(q14.3), Monosomy 5q14.3. Tomeko brings together the specialists, research, clinical trials, treatments and community for 5q14.3 microdeletion syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:228384 · OMIM 613443 · ICD-10 Q93.5 · GARD 0012166
Start by learning the basics from an authoritative source, find a specialist or center that sees 5q14.3 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 5q14.3 microdeletion syndrome, filtered to your area.
Tomeko shows live, recruiting studies for 5q14.3 microdeletion syndrome from ClinicalTrials.gov on the hub.