Oculomaxillofacial dysostosis

Introduction: Oculomaxillofacial dysostosis

Description of Oculomaxillofacial dysostosis

Oculomaxillofacial dysostosis (medical condition): A very rare syndrome characterized mainly by eye, jaw and facial abnormalities.

See also:

Oculomaxillofacial dysostosis:
  »Introduction: Oculomaxillofacial dysostosis
  »Symptoms of Oculomaxillofacial dysostosis

Oculomaxillofacial dysostosis: Related Topics

These medical condition or symptom topics may be relevant to medical information for Oculomaxillofacial dysostosis:

• Dysostosis

Oculomaxillofacial dysostosis: Rare Disease

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

Oculomaxillofacial dysostosis is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Oculomaxillofacial dysostosis, or a subtype of Oculomaxillofacial dysostosis, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Oculomaxillofacial dysostosis as a "rare disease".

Source - Orphanet

Oculomaxillofacial dysostosis as a Disease

Oculomaxillofacial dysostosis (medical condition): See Oculomaxillofacial dysostosis (disease information).
  »Introduction: Oculomaxillofacial dysostosis
  »Symptoms of Oculomaxillofacial dysostosis

More information on medical condition: Oculomaxillofacial dysostosis:

• Information about Oculomaxillofacial dysostosis
• Basic Summary for Oculomaxillofacial dysostosis
• Symptoms of Oculomaxillofacial dysostosis

Terms associated with Oculomaxillofacial dysostosis:

Terms Similar to Oculomaxillofacial dysostosis:

• Oblique facial clefts
• Oculomaxillofacial dysplasia with oblique facial clefts
• Richieri Costa Gorlin syndrome

Source - NIH

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