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MGA 3

Introduction: MGA 3

Description of MGA 3

MGA 3 (medical condition): A rare genetic condition where a gene mutation prevents...more »

See also:

3 alpha methylglutaconicaciduria, type 3:
  »Introduction: 3 alpha methylglutaconicaciduria, type 3
  »Symptoms of 3 alpha methylglutaconicaciduria, type 3

MGA 3: Rare Disease

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

MGA 3 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that MGA 3, or a subtype of MGA 3, 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 MGA 3 as a "rare disease".

Source - Orphanet

MGA 3 as a Disease

MGA 3: Another name for 3 alpha methylglutaconicaciduria, type 3 (or close medical condition association).
  »Introduction: 3 alpha methylglutaconicaciduria, type 3
  »Symptoms of 3 alpha methylglutaconicaciduria, type 3

MGA 3: Related Diseases

MGA 3: MGA 3 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of MGA 3 (3 alpha methylglutaconicaciduria, type 3)

Some of the symptoms of MGA 3 incude:

MGA 3: Related Disease Topics

These medical disease topics may be related to MGA 3:

Terms associated with MGA 3:

Terms Similar to MGA 3:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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