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Dictionary » Familial pyrimidinemia
 

Familial pyrimidinemia

Introduction: Familial pyrimidinemia

Description of Familial pyrimidinemia

Familial pyrimidinemia (medical condition): A metabolic error where a deficiency of an enzyme called...more »

See also:

Dihydropyrimidine dehydrogenase deficiency:
  »Introduction: Dihydropyrimidine dehydrogenase deficiency
  »Symptoms of Dihydropyrimidine dehydrogenase deficiency

Familial pyrimidinemia: Related Topics

These medical condition or symptom topics may be relevant to medical information for Familial pyrimidinemia:

Familial pyrimidinemia: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

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 as a Disease

Familial pyrimidinemia: Another name for Dihydropyrimidine dehydrogenase deficiency (or close medical condition association).
  »Introduction: Dihydropyrimidine dehydrogenase deficiency
  »Symptoms of Dihydropyrimidine dehydrogenase deficiency

Familial pyrimidinemia: Related Diseases

Familial pyrimidinemia: Familial pyrimidinemia is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Familial pyrimidinemia (Dihydropyrimidine dehydrogenase deficiency)

Some of the symptoms of Familial pyrimidinemia incude:

Familial pyrimidinemia: Related Disease Topics

These medical disease topics may be related to Familial pyrimidinemia:

Terms associated with Familial pyrimidinemia:

Terms Similar to Familial pyrimidinemia:

Source - NIH

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