Assessment
Questionnaire
Have a symptom?
See what questions
a doctor would ask.
See what questions
a doctor would ask.
Methylmalonicaciduria with homocystinuria, cobalamin F: An inherited organic acid disorder where an enzyme deficiency (cbl F) impairs the body's ability to break down certain proteins (methionine, threonine, isoleucine and valine) consumed in the diet. This results in a buildup of methylmalonic acid and homocystine which results in harmful affects. More detailed information about the symptoms, causes, and treatments of Methylmalonicaciduria with homocystinuria, cobalamin F is available below.
See full list of 23 symptoms of Methylmalonicaciduria with homocystinuria, cobalamin F
Review possible medical complications related to Methylmalonicaciduria with homocystinuria, cobalamin F:
Read more about causes of Methylmalonicaciduria with homocystinuria, cobalamin F.
Research the causes of these diseases that are similar to, or related to, Methylmalonicaciduria with homocystinuria, cobalamin F:
Types of Methylmalonicaciduria with homocystinuria, cobalamin F
Read about other experiences, ask a question about Methylmalonicaciduria with homocystinuria, cobalamin F, or answer someone else's question, on our message boards:
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 © 2011 Health Grades Inc. All rights reserved. Last Update: 1 February, 2012 (4:52)