Just diagnosed with Okihiro syndrome due to 20q13 microdeletion?
You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Okihiro syndrome due to 20q13 microdeletion, look for clinical trials, and connect with others living with it — all in one place.
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Okihiro syndrome due to 20q13 microdeletion is a rare condition. Also known as Duane-radial ray syndrome due to monosomy 20q13, Okihiro syndrome due to del(20)(q13), Okihiro syndrome due to monosomy 20q13. Tomeko brings together the specialists, research, clinical trials, treatments and community for Okihiro syndrome due to 20q13 microdeletion so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:261638 · OMIM 607323 · ICD-10 Q87.8 · GARD 0020787
Find care for Okihiro syndrome due to 20q13 microdeletion
Authoritative references for Okihiro syndrome due to 20q13 microdeletion
Research & market landscape for Okihiro syndrome due to 20q13 microdeletion
Following Okihiro syndrome due to 20q13 microdeletion for research or industry? Tomeko brings together the recruiting trials, the latest literature, patient organizations, and the specialist and care-center footprint for Okihiro syndrome due to 20q13 microdeletion — the real-world landscape behind the condition, in one place.
- Latest Okihiro syndrome due to 20q13 microdeletion research on PubMed ↗
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Common questions
What is Okihiro syndrome due to 20q13 microdeletion?
Okihiro syndrome due to 20q13 microdeletion is a rare condition. Also known as Duane-radial ray syndrome due to monosomy 20q13, Okihiro syndrome due to del(20)(q13), Okihiro syndrome due to monosomy 20q13. For an authoritative medical description see the reference sources on this page; Tomeko brings the specialists, clinical trials, patient organizations and community for Okihiro syndrome due to 20q13 microdeletion together in one place.
What are the symptoms of Okihiro syndrome due to 20q13 microdeletion?
Symptoms of Okihiro syndrome due to 20q13 microdeletion 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 Okihiro syndrome due to 20q13 microdeletion.
How is Okihiro syndrome due to 20q13 microdeletion treated?
Treatment for Okihiro syndrome due to 20q13 microdeletion depends on the individual and is managed by specialists. Use Tomeko to find clinicians and Centers of Excellence who see Okihiro syndrome due to 20q13 microdeletion, and review current options with them.
What causes Okihiro syndrome due to 20q13 microdeletion — is it genetic?
The cause and inheritance of Okihiro syndrome due to 20q13 microdeletion are described in the authoritative references linked on this page. A genetics or specialist clinician who treats Okihiro syndrome due to 20q13 microdeletion can explain what it means for you and your family.
I was just diagnosed with Okihiro syndrome due to 20q13 microdeletion — what should I do first?
Start by learning the basics from an authoritative source, find a specialist or center that sees Okihiro syndrome due to 20q13 microdeletion, and connect with a patient organization. Tomeko brings these together on one hub.
Where can I find a specialist for Okihiro syndrome due to 20q13 microdeletion?
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Okihiro syndrome due to 20q13 microdeletion, filtered to your area.
Are there clinical trials for Okihiro syndrome due to 20q13 microdeletion?
Tomeko shows live, recruiting studies for Okihiro syndrome due to 20q13 microdeletion from ClinicalTrials.gov on the hub.
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