Acromesomelic dysplasia Hunter Thompson type: A rare genetic syndrome characterized by various severe developmental abnormalities of the skeletal bones. More detailed information about the symptoms, causes, and treatments of Acromesomelic dysplasia Hunter Thompson type is available below.
See full list of 22 symptoms of Acromesomelic dysplasia Hunter Thompson type
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Acromesomelic dysplasia Hunter Thompson type is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Acromesomelic dysplasia Hunter Thompson type, or a subtype of Acromesomelic dysplasia Hunter Thompson type,
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 Acromesomelic dysplasia Hunter Thompson type as a "rare disease".
Source - Orphanet
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