Acrocephalopolysyndactyly type 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 Acrocephalopolysyndactyly type III is available below.
See full list of 36 symptoms of Acrocephalopolysyndactyly type III
Read more about causes of Acrocephalopolysyndactyly type III.
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Read more about Misdiagnosis and Acrocephalopolysyndactyly type III
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Types of Acrocephalopolysyndactyly type III
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Acrocephalopolysyndactyly type III is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Acrocephalopolysyndactyly type III, or a subtype of Acrocephalopolysyndactyly type III,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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