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Dictionary » Guadalajara camptodactyly syndrome type 2
 

Guadalajara camptodactyly syndrome type 2

Introduction: Guadalajara camptodactyly syndrome type 2

Description of Guadalajara camptodactyly syndrome type 2

Guadalajara camptodactyly syndrome type 2 (medical condition): A rare syndrome characterized mainly by retarded...more »

See also:

Camptodactyly syndrome, Guadalajara type 2:
  »Introduction: Camptodactyly syndrome, Guadalajara type 2
  »Symptoms of Camptodactyly syndrome, Guadalajara type 2

Guadalajara camptodactyly syndrome type 2: Related Topics

These medical condition or symptom topics may be relevant to medical information for Guadalajara camptodactyly syndrome type 2:

Guadalajara camptodactyly syndrome type 2: Rare Disease

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

Guadalajara camptodactyly syndrome 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 Guadalajara camptodactyly syndrome type 2, or a subtype of Guadalajara camptodactyly syndrome type 2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Guadalajara camptodactyly syndrome type 2 as a Disease

Guadalajara camptodactyly syndrome type 2: Another name for Camptodactyly syndrome, Guadalajara type 2 (or close medical condition association).
  »Introduction: Camptodactyly syndrome, Guadalajara type 2
  »Symptoms of Camptodactyly syndrome, Guadalajara type 2

Guadalajara camptodactyly syndrome type 2: Related Diseases

Guadalajara camptodactyly syndrome type 2: Guadalajara camptodactyly syndrome type 2 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Guadalajara camptodactyly syndrome type 2 (Camptodactyly syndrome, Guadalajara type 2)

Some of the symptoms of Guadalajara camptodactyly syndrome type 2 incude:

Terms associated with Guadalajara camptodactyly syndrome type 2:

Terms Similar to Guadalajara camptodactyly syndrome type 2:

Source - NIH

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