Just diagnosed with Monosomy 22?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Monosomy 22, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Monosomy 22 hub →Overview
Monosomy 22 is a rare condition. Also known as Del(22), Deletion 22. Tomeko brings together the specialists, research, clinical trials, treatments and community for Monosomy 22 so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:96123 · ICD-10 Q93.0 · GARD 0019324
Find care for Monosomy 22
Authoritative references for Monosomy 22
Research & market landscape for Monosomy 22
Following Monosomy 22 for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Monosomy 22 — the real-world landscape behind the condition, in one place.
- Latest Monosomy 22 research on PubMed ↗
- Recruiting Monosomy 22 trials on ClinicalTrials.gov ↗
- Explore the Monosomy 22 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 Monosomy 22 and every rare condition. See how Tomeko works with industry →
Common questions
What is Monosomy 22?
Monosomy 22 is a rare condition. Also known as Del(22), Deletion 22. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Monosomy 22 together in one place.
What are the symptoms of Monosomy 22?
Symptoms of Monosomy 22 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 Monosomy 22.
How is Monosomy 22 treated?
Treatment for Monosomy 22 depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Monosomy 22, and review current options with them.
What causes Monosomy 22 — is it genetic?
The cause and inheritance of Monosomy 22 are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Monosomy 22 can explain what it means for you and your family.
I was just diagnosed with Monosomy 22 — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Monosomy 22, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Monosomy 22?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Monosomy 22, filtered to your area.
Are there clinical trials for Monosomy 22?
Tomeko shows live, recruiting studies for Monosomy 22 from ClinicalTrials.gov on the hub.
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