Arthrogryposis multiplex congenita, distal, X-linked: A rare condition characterized by the presence of contractures at birth as well as various other anomalies. The condition is X-linked. More detailed information about the symptoms, causes, and treatments of Arthrogryposis multiplex congenita, distal, X-linked is available below.
See full list of 22 symptoms of Arthrogryposis multiplex congenita, distal, X-linked
Read more about causes of Arthrogryposis multiplex congenita, distal, X-linked.
See full list of 11 occasional symptoms of Arthrogryposis multiplex congenita, distal, X-linked
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Read more about Misdiagnosis and Arthrogryposis multiplex congenita, distal, X-linked
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Arthrogryposis multiplex congenita, distal, X-linked is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Arthrogryposis multiplex congenita, distal, X-linked, or a subtype of Arthrogryposis multiplex congenita, distal, X-linked,
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 Arthrogryposis multiplex congenita, distal, X-linked as a "rare disease".
Source - Orphanet
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