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MGA1

Introduction: MGA1

Description of MGA1

MGA1 (medical condition): A rare inherited disorder characterized by vitamin B12...more »

See also:

Megaloblasti Anemia, 1:
  »Introduction: Megaloblasti Anemia, 1
  »Symptoms of Megaloblasti Anemia, 1
  »Treatments for Megaloblasti Anemia, 1

MGA1: Rare Disease

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

MGA1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that MGA1, or a subtype of MGA1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

MGA1 as a Disease

MGA1: Another name for Megaloblasti Anemia, 1 (or close medical condition association).
  »Introduction: Megaloblasti Anemia, 1
  »Symptoms of Megaloblasti Anemia, 1
  »Treatments for Megaloblasti Anemia, 1

MGA1: Related Diseases

MGA1: MGA1 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of MGA1 (Megaloblasti Anemia, 1)

Some of the symptoms of MGA1 incude:

Treatments for MGA1 (Megaloblasti Anemia, 1)

Treatments for MGA1 (Megaloblasti Anemia, 1) include:

  • Lifelong Vitamin B12 supplements are needed - must be injected as the intestines are unable to absorb the vitamin. Excessive protein in the urine will persist despite treatment but does not signal kidney problems.

Treatment of MGA1: For more treatment information about MGA1, see treatment of Megaloblasti Anemia, 1 (MGA1)

Terms associated with MGA1:

Terms Similar to MGA1:

Source - NIH

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