Omenn syndrome: Introduction
Omenn syndrome: A rare inherited disorder of the immune system involving B and T lymphocytes and characterized by skin rash and frequent infections.
More detailed information about the symptoms,
causes, and treatments of Omenn syndrome is available below.
Symptoms of Omenn syndrome
See full list of 13
symptoms of Omenn syndrome
Wrongly Diagnosed with Omenn syndrome?
Omenn syndrome: Complications
Review possible medical complications related to Omenn syndrome:
Causes of Omenn syndrome
Read more about causes of Omenn syndrome.
Disease Topics Related To Omenn syndrome
Research the causes of these diseases that are similar to, or related to, Omenn syndrome:
Misdiagnosis and Omenn syndrome
Psoriasis often undiagnosed cause of skin symptoms in children: Children who suffer
from the skin disorder called psoriasis can often go undiagnosed.
The main problem is that psoriasis is rare in children, and not often
seen...read more »
Read more about Misdiagnosis and Omenn syndrome
Omenn syndrome: Research Doctors & Specialists
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Evidence Based Medicine Research for Omenn syndrome
Medical research articles related to Omenn syndrome include:
Click here to find more evidence-based articles on the TRIP Database
Omenn syndrome: Animations
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Prognosis for Omenn syndrome
Prognosis for Omenn syndrome:
More about prognosis of Omenn syndrome
Research about Omenn syndrome
Visit our research pages for current research about Omenn syndrome treatments.
Statistics for Omenn syndrome
Omenn syndrome: Broader Related Topics
Types of Omenn syndrome
User Interactive Forums
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Definitions of Omenn syndrome:
Omenn syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Omenn syndrome, or a subtype of Omenn syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Omenn syndrome as a "rare disease".
Source - Orphanet
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