You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Frias syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full Frias syndrome hub →Frias syndrome is a rare condition. Also known as Frias syndrome, 14q22-q23 microdeletion syndrome, Del(14)(q22q23), Monosomy 14q22-q23, Monosomy 14q22q23. Tomeko brings together the specialists, research, clinical trials, treatments and community for Frias syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:2055 · OMIM 609640 · ICD-10 Q93.5 · GARD 0002384
Start by learning the basics from an authoritative source, find a specialist or center that sees Frias 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 Frias syndrome, filtered to your area.
Tomeko shows live, recruiting studies for Frias syndrome from ClinicalTrials.gov on the hub.