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ACPS III: A rare genetic condition characterized by head and digital anomalies as well as other abnormalities. More detailed information about the symptoms, causes, and treatments of ACPS III is available below.
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ACPS III is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that ACPS III, or a subtype of ACPS III,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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