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Dictionary » Oculomelic amyoplasia

Oculomelic amyoplasia

Introduction: Oculomelic amyoplasia

Description of Oculomelic amyoplasia

Oculomelic amyoplasia (medical condition): A rare genetic disorder characterized by limb contractures (tightening of...more »

See also:

Oculomelic amyoplasia:
  »Introduction: Oculomelic amyoplasia
  »Symptoms of Oculomelic amyoplasia

Oculomelic amyoplasia: Related Topics

These medical condition or symptom topics may be relevant to medical information for Oculomelic amyoplasia:

Oculomelic amyoplasia: Rare Disease

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

Oculomelic amyoplasia is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Oculomelic amyoplasia, or a subtype of Oculomelic amyoplasia, 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 if affects 1 person per 2,000. They list Oculomelic amyoplasia as a "rare disease".

Source - Orphanet

Oculomelic amyoplasia as a Disease

Oculomelic amyoplasia (medical condition): See Oculomelic amyoplasia (disease information).
  »Introduction: Oculomelic amyoplasia
  »Symptoms of Oculomelic amyoplasia

Oculomelic amyoplasia: Related Diseases

Oculomelic amyoplasia: Oculomelic amyoplasia is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: Oculomelic amyoplasia:

Oculomelic amyoplasia: Related Disease Topics

These medical disease topics may be related to Oculomelic amyoplasia:

Terms associated with Oculomelic amyoplasia:

Terms Similar to Oculomelic amyoplasia:

Source - NIH

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