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Familial pyrimidinemia (medical condition): A metabolic error where a deficiency of an enzyme called dihydropyrimidine...more »
These medical condition or symptom topics may be relevant to medical information for Familial pyrimidinemia:
Familial pyrimidinemia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Familial pyrimidinemia, or a subtype of Familial pyrimidinemia,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Familial pyrimidinemia: Another name for Dihydropyrimidine dehydrogenase deficiency (or close medical condition association).
»Introduction: Dihydropyrimidine dehydrogenase deficiency
»Symptoms of Dihydropyrimidine dehydrogenase deficiency
Familial pyrimidinemia: Familial pyrimidinemia is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Familial pyrimidinemia incude:
These medical disease topics may be related to Familial pyrimidinemia:
Source - NIH
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