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Dictionary » Familial Caffey's disease
 

Familial Caffey's disease

Introduction: Familial Caffey's disease

Description of Familial Caffey's disease

Familial Caffey's disease (medical condition): A rare inflammatory disorder that affects bones and soft tissue in infants....more »

See also:

Hyperostosis cortical infantile:
  »Introduction: Hyperostosis cortical infantile
  »Symptoms of Hyperostosis cortical infantile

Familial Caffey's disease: Related Topics

These medical condition or symptom topics may be relevant to medical information for Familial Caffey's disease:

Familial Caffey's disease: Rare Disease

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

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

Familial Caffey's disease as a Disease

Familial Caffey's disease: Another name for Hyperostosis cortical infantile (or close medical condition association).
  »Introduction: Hyperostosis cortical infantile
  »Symptoms of Hyperostosis cortical infantile

Familial Caffey's disease: Related Diseases

Familial Caffey's disease: Familial Caffey's disease is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Familial Caffey's disease (Hyperostosis cortical infantile)

Some of the symptoms of Familial Caffey's disease incude:

Terms associated with Familial Caffey's disease:

Terms Similar to Familial Caffey's disease:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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