CDG1B

Introduction: CDG1B

Description of CDG1B

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

• Genetic conditions
• Metabolic conditions
• Congenital conditions - metabolic disorders
• Congenital conditions

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

Some of the symptoms of CDG1B incude:

• Liver disease
• Coagulopathy
• Protein-losing enteropathy
• Cyclic vomiting
• Diarrhea

See full list of 8 symptoms of CDG1B (Congenital disorder of glycosylation type 1B)

CDG1B: Related Disease Topics

These medical disease topics may be related to CDG1B:

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

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Medical dictionaries:

• Medical dictionary,
• Medical Acronymns/Abbreviations

More Medical Dictionary Topics

Prespondylolisthesis

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