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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.
See full list of 36 symptoms of ACPS III
Read more about causes of ACPS III.
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Read more about Misdiagnosis and ACPS III
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Types of ACPS III
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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)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list ACPS III as a "rare disease".
Source - Orphanet
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