Inborn aminoacid metabolism disorder

Introduction: Inborn aminoacid metabolism disorder

Description of Inborn aminoacid metabolism disorder

Inborn aminoacid metabolism disorder (medical condition): A group of inherited disorders where the body is not able...more »

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Inborn amino acid metabolism disorder:
  »Introduction: Inborn amino acid metabolism disorder
  »Symptoms of Inborn amino acid metabolism disorder
  »Treatments for Inborn amino acid metabolism disorder

Inborn aminoacid metabolism disorder: disorders affecting amino acid metabolism; majority of these disorders are inherited and present in the neonatal period with metabolic disturbances (for example, acidosis) and neurologic manifestations; present at birth, although they may not become symptomatic until later in life.
Source: CRISP

Inborn aminoacid metabolism disorder: Related Topics

These medical condition or symptom topics may be relevant to medical information for Inborn aminoacid metabolism disorder:

• Aminoacid metabolism
• Metabolism disorder
• Inborn
• Aminoacid
• Metabolism
• Disorder
• Acid
• Inherited
• Inherited disease
• Inherited disorder

Inborn aminoacid metabolism disorder: Rare Disease

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

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

Inborn aminoacid metabolism disorder as a Disease

Inborn aminoacid metabolism disorder (medical condition): See Inborn amino acid metabolism disorder (disease information).
  »Introduction: Inborn amino acid metabolism disorder
  »Symptoms of Inborn amino acid metabolism disorder
  »Treatments for Inborn amino acid metabolism disorder

Inborn aminoacid metabolism disorder: Related Diseases

Inborn aminoacid metabolism disorder: Inborn aminoacid metabolism disorder is listed as a type of (or associated with) the following medical conditions in our database:

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

More information on medical condition: Inborn amino acid metabolism disorder:

• Information about Inborn amino acid metabolism disorder
• Basic Summary for Inborn amino acid metabolism disorder
• Symptoms of Inborn amino acid metabolism disorder
• Complications of Inborn amino acid metabolism disorder
• Treatments for Inborn amino acid metabolism disorder

Terms associated with Inborn aminoacid metabolism disorder:

Terms Similar to Inborn aminoacid metabolism disorder:

• Amino acid metabolism, inborn errors

Source - NIH

More specific terms for Inborn aminoacid metabolism disorder:

• albinism
• cystinosis
• cystinuria
• histidinemia
• homocystinuria
• hyperglycinemia
• hyperphenylalaninemia
• inborn renal aminoaciduria
• inborn urea cycle disorder
• isovaleric acidemia
• maple syrup urine disease
• methylmalonic aciduria
• ornithinemia
• phenylketonuria
• tyrosinemia

Source - CRISP

Broader terms for Inborn aminoacid metabolism disorder

• inborn metabolism disorder

Source - CRISP

The term Inborn aminoacid metabolism disorder can be used for:

• cystathionase deficiency
• cystathioninuria
• homoserine deaminase deficiency
• hyperlysinemia
• inborn aminoacidopathy
• inborn aminoaciduria
• lysinemia

Source: CRISP

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