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AGS1

Introduction: AGS1

Description of AGS1

AGS1 (medical condition): A rare inherited progressive disease that affects the brain and...more »

See also:

Aicardi-Goutieres syndrome 1:
  »Introduction: Aicardi-Goutieres syndrome 1
  »Symptoms of Aicardi-Goutieres syndrome 1

AGS1: Rare Disease

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

AGS1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that AGS1, or a subtype of AGS1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

AGS1 as a Disease

AGS1: Another name for Aicardi-Goutieres syndrome 1 (or close medical condition association).
  »Introduction: Aicardi-Goutieres syndrome 1
  »Symptoms of Aicardi-Goutieres syndrome 1

AGS1: Related Diseases

AGS1: AGS1 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of AGS1 (Aicardi-Goutieres syndrome 1)

Some of the symptoms of AGS1 incude:

Terms associated with AGS1:

Terms Similar to AGS1:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

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  • Glutamate formiminotransferase deficiency
  • Glutamate formiminotrransferase deficiency
  • Glutamate Plasma Membrane Transport Proteins
  • Glutamate receptor
  • Glutamate Synthase
  • Glutamate Synthase (NADH)
  • Glutamate synthetase
  • Glutamate transporter
  • Glutamate-5-Semialdehyde Dehydrogenase

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