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MGA 3 (medical condition): A rare genetic condition where a gene mutation prevents...more »
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, 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: 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: MGA 3 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of MGA 3 incude:
These medical disease topics may be related to MGA 3:
Source - NIH
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