Just diagnosed with Frias syndrome?
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 interactive Frias syndrome hub →Overview
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
Find care for Frias syndrome
Authoritative references for Frias syndrome
Research & market landscape for Frias syndrome
Following Frias syndrome for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Frias syndrome — the real-world landscape behind the condition, in one place.
- Latest Frias syndrome research on PubMed ↗
- Recruiting Frias syndrome trials on ClinicalTrials.gov ↗
- Explore the Frias syndrome research & specialist footprint on Tomeko
Researchers, patient organizations & industry: Tomeko provides de-identified, no-PHI demand and engagement signal, trial awareness, and a labeled, editorially-firewalled presence for Frias syndrome and every rare condition. See how Tomeko works with industry →
Common questions
What is Frias syndrome?
Frias syndrome is a rare condition. Also known as Frias syndrome, 14q22-q23 microdeletion syndrome, Del(14)(q22q23), Monosomy 14q22-q23, Monosomy 14q22q23. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Frias syndrome together in one place.
What are the symptoms of Frias syndrome?
Symptoms of Frias syndrome vary from person to person. For a reviewed, plain-language overview see the authoritative references below (NIH GARD, Orphanet), and discuss your own symptoms with a clinician who treats Frias syndrome.
How is Frias syndrome treated?
Treatment for Frias syndrome depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Frias syndrome, and review current options with them.
What causes Frias syndrome — is it genetic?
The cause and inheritance of Frias syndrome are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Frias syndrome can explain what it means for you and your family.
I was just diagnosed with Frias syndrome — what should I do first?
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.
Where can I find a specialist for Frias syndrome?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Frias syndrome, filtered to your area.
Are there clinical trials for Frias syndrome?
Tomeko shows live, recruiting studies for Frias syndrome from ClinicalTrials.gov on the hub.
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