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ACS3 (medical condition): A rare genetic disorder characterized by premature joining of certain...more »
ACS3 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that ACS3, or a subtype of ACS3,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
ACS3: ACS3 is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of ACS3 incude:
These medical disease topics may be related to ACS3:
Source - NIH
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