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Dictionary » CDG1B


Introduction: CDG1B

Description of CDG1B

CDG1B (medical condition): A very rare inherited metabolic disorder where defective carbohydrate...more »

See also:

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

CDG1B as a Disease

CDG1B: Another name for Congenital disorder of glycosylation type 1B (or close medical condition association).
  »Introduction: Congenital disorder of glycosylation type 1B
  »Symptoms of Congenital disorder of glycosylation type 1B

CDG1B: Related Diseases

CDG1B: CDG1B is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of CDG1B (Congenital disorder of glycosylation type 1B)

Some of the symptoms of CDG1B incude:

CDG1B: Related Disease Topics

These medical disease topics may be related to CDG1B:

  • congenital disorder of glycosylation
  • autosomal recessive disorders
  • Jaeken syndrome
  • multisystem disorder

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

  • Oppenheim disease
  • Oppenheim reflex
  • Oppenheim syndrome
  • Oppenheim's disease
  • Oppenheim's syndrome
  • OPPG
  • Oppilative
  • Opponens
  • Opponens digiti minimi pedis (muscle)
  • Opponens muscle
  • Opponent color
  • Opportunistic
  • Opportunistic infection
  • Opportunistic mycoses

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