CPO deficiency (medical condition): An inherited metabolic disorder involving a deficiency of coproporphyrinogen oxidase. The condition is similar to but milder than intermittent porphyria and sometimes includes photosensitivity.
See also:
Dobriner syndrome:
»Introduction: Dobriner syndrome
»Symptoms of Dobriner syndrome
These medical condition or symptom topics may be relevant to medical information for CPO deficiency:
CPO deficiency is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that CPO deficiency, or a subtype of CPO deficiency,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
CPO deficiency: Another name for Dobriner syndrome (or close medical condition association).
»Introduction: Dobriner syndrome
»Symptoms of Dobriner syndrome
Some of the symptoms of CPO deficiency incude:
See full list of 19 symptoms of CPO deficiency (Dobriner syndrome)
These medical disease topics may be related to CPO deficiency:
Source - NIH
Search to find out more about CPO deficiency:
|
What do you think about the features of this website? Take our user survey and have your say:
Tools & Services:
Medical Articles:
Search Specialists by State and City
By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.
Copyright © 2009 Health Grades Inc. All rights reserved.
