Just diagnosed with Chromosome 17p deletion?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Chromosome 17p deletion, look for clinical trials, and connect with others living with it — all in one place.
Open the full interactive Chromosome 17p deletion hub →Overview
Chromosome 17p deletion is a rare condition. Also known as Partial deletion of chromosome 17p, Partial monosomy of chromosome 17p, Partial monosomy of the short arm of chromosome 17. Tomeko brings together the specialists, research, clinical trials, treatments and community for Chromosome 17p deletion so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:261965 · GARD 0020817
Find care for Chromosome 17p deletion
Authoritative references for Chromosome 17p deletion
Research & market landscape for Chromosome 17p deletion
Following Chromosome 17p deletion for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Chromosome 17p deletion — the real-world landscape behind the condition, in one place.
- Latest Chromosome 17p deletion research on PubMed ↗
- Recruiting Chromosome 17p deletion trials on ClinicalTrials.gov ↗
- Explore the Chromosome 17p deletion 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 Chromosome 17p deletion and every rare condition. See how Tomeko works with industry →
Common questions
What is Chromosome 17p deletion?
Chromosome 17p deletion is a rare condition. Also known as Partial deletion of chromosome 17p, Partial monosomy of chromosome 17p, Partial monosomy of the short arm of chromosome 17. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Chromosome 17p deletion together in one place.
What are the symptoms of Chromosome 17p deletion?
Symptoms of Chromosome 17p deletion 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 Chromosome 17p deletion.
How is Chromosome 17p deletion treated?
Treatment for Chromosome 17p deletion depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Chromosome 17p deletion, and review current options with them.
What causes Chromosome 17p deletion — is it genetic?
The cause and inheritance of Chromosome 17p deletion are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Chromosome 17p deletion can explain what it means for you and your family.
I was just diagnosed with Chromosome 17p deletion — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Chromosome 17p deletion, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Chromosome 17p deletion?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Chromosome 17p deletion, filtered to your area.
Are there clinical trials for Chromosome 17p deletion?
Tomeko shows live, recruiting studies for Chromosome 17p deletion from ClinicalTrials.gov on the hub.
Related conditions
Other conditions on Tomeko you may be looking for:
- Chromosome 16q22 deletion syndrome
- Chromosome 17p13.1 deletion syndrome
- Chromosome 16q12 duplication syndrome
- Chromosome 17p13.3 duplication syndrome
- Chromosome 16p13.3 duplication syndrome
- Chromosome 17P13.3, telomeric, duplication syndrome
- Chromosome 16p13.3 deletion syndrome
- Chromosome 17q11.2 deletion syndrome, 1.4Mb