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ACG1A (medical condition): A rare genetic disorder characterized by abnormal cartilage formation and...more »
ACG1A is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that ACG1A, or a subtype of ACG1A,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
ACG1A: ACG1A is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of ACG1A incude:
Source - NIH
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