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Dictionary » Gyrate atrophy
 

Gyrate atrophy

Introduction: Gyrate atrophy

Description of Gyrate atrophy

Gyrate atrophy (medical condition): Excessive levels of ornithine in the blood caused by a...more »

See also:

Hyperornithinemia:
  »Introduction: Hyperornithinemia
  »Symptoms of Hyperornithinemia

Gyrate atrophy: Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.
Source: MeSH 2007

Gyrate atrophy: Related Topics

These medical condition or symptom topics may be relevant to medical information for Gyrate atrophy:

Gyrate atrophy: Rare Disease

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

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

Gyrate atrophy as a Disease

Gyrate atrophy: Another name for Hyperornithinemia (or close medical condition association).
  »Introduction: Hyperornithinemia
  »Symptoms of Hyperornithinemia

Gyrate atrophy: Related Diseases

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

Symptoms of Gyrate atrophy (Hyperornithinemia)

Some of the symptoms of Gyrate atrophy incude:

Gyrate atrophy: Related Disease Topics

These medical disease topics may be related to Gyrate atrophy:

Hierarchical classifications of Gyrate atrophy

The following list attempts to classify Gyrate atrophy into categories where each line is subset of the next.

MeSH 2007 Hierarchy:

MeSH 2007 Hierarchy

MeSH 2007 Hierarchy

Interesting Medical Articles:

Medical dictionaries:

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