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Dictionary » CDG syndrome
 

CDG syndrome

Introduction: CDG syndrome

Description of CDG syndrome

CDG syndrome (medical condition): A very rare inherited metabolic disorder where defective...more »

See also:

Congenital disorder of glycosylation type 1A:
  »Introduction: Congenital disorder of glycosylation type 1A
  »Symptoms of Congenital disorder of glycosylation type 1A

CDG syndrome: Related Topics

These medical condition or symptom topics may be relevant to medical information for CDG syndrome:

CDG syndrome: Rare Disease

Ophanet

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

Source - Orphanet

CDG syndrome as a Disease

CDG syndrome: Another name for Congenital disorder of glycosylation type 1A (or close medical condition association).
  »Introduction: Congenital disorder of glycosylation type 1A
  »Symptoms of Congenital disorder of glycosylation type 1A

CDG syndrome: Related Diseases

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

Symptoms of CDG syndrome (Congenital disorder of glycosylation type 1A)

Some of the symptoms of CDG syndrome incude:

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

  • Nucleic acid binding protein
  • Nucleic acid biosynthesis
  • Nucleic acid chemical synthesis
  • Nucleic acid cloning
  • Nucleic Acid Conformation
  • Nucleic acid denaturation
  • Nucleic acid detection
  • Nucleic Acid Heteroduplexes
  • Nucleic acid hybridization
  • Nucleic acid inhibitor

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