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Dictionary » Spondylometaphyseal dysplasia, Algerian type
 

Spondylometaphyseal dysplasia, Algerian type

Introduction: Spondylometaphyseal dysplasia, Algerian type

Description of Spondylometaphyseal dysplasia, Algerian type

Spondylometaphyseal dysplasia, Algerian type (medical condition): A severe, dominantly inherited skeletal disorder involving...more »

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Spondylometaphyseal dysplasia, Algerian type:
  »Introduction: Spondylometaphyseal dysplasia, Algerian type
  »Symptoms of Spondylometaphyseal dysplasia, Algerian type

Spondylometaphyseal dysplasia, Algerian type: Related Topics

These medical condition or symptom topics may be relevant to medical information for Spondylometaphyseal dysplasia, Algerian type:

Spondylometaphyseal dysplasia, Algerian type: Rare Disease

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

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

Spondylometaphyseal dysplasia, Algerian type as a Disease

Spondylometaphyseal dysplasia, Algerian type (medical condition): See Spondylometaphyseal dysplasia, Algerian type (disease information).
  »Introduction: Spondylometaphyseal dysplasia, Algerian type
  »Symptoms of Spondylometaphyseal dysplasia, Algerian type

Spondylometaphyseal dysplasia, Algerian type: Related Diseases

Spondylometaphyseal dysplasia, Algerian type: Spondylometaphyseal dysplasia, Algerian type is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: Spondylometaphyseal dysplasia, Algerian type:

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