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Dictionary » Arthrogryposis multiplex congenita, distal type 2
 

Arthrogryposis multiplex congenita, distal type 2

Arthrogryposis multiplex congenita, distal type 2: Related Topics

These medical condition or symptom topics may be relevant to medical information for Arthrogryposis multiplex congenita, distal type 2:

Arthrogryposis multiplex congenita, distal type 2: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Arthrogryposis multiplex congenita, distal type 2 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 type 2, or a subtype of Arthrogryposis multiplex congenita, distal type 2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Terms associated with Arthrogryposis multiplex congenita, distal type 2:

Terms Similar to Arthrogryposis multiplex congenita, distal type 2:

Source - NIH

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