4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency

Introduction: 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency

Description of 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency (medical condition): A very rare metabolic disorder where a deficiency...more »

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4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency:
  »Introduction: 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency
  »Symptoms of 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency: Related Topics

These medical condition or symptom topics may be relevant to medical information for 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency:

• Hydroxylase
• Deficiency
• Deficiency disease

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency: Rare Disease

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

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency, or a subtype of 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency as a "rare disease".

Source - Orphanet

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency as a Disease

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency (medical condition): See 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency (disease information).
  »Introduction: 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency
  »Symptoms of 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency: Related Diseases

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency: 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency is listed as a type of (or associated with) the following medical conditions in our database:

• Genetic conditions
• Metabolic conditions
• Congenital conditions - metabolic disorders
• Congenital conditions

More information on medical condition: 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency:

• Information about 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency
• Basic Summary for 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency
• Symptoms of 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency

4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency: Related Disease Topics

These medical disease topics may be related to 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency:

• autosomal dominant disorder
• metabolic acidosis
• tyrosinemia
• Hawkinsinuria

Terms associated with 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency:

Terms Similar to 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency:

• Hawkinsinuria

Source - NIH

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