CDG1m

Introduction: CDG1m

Description of CDG1m

CDG1m (medical condition): Congenital disorders of glycosylation is a group of very rare inherited...more »

See also:

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

CDG1m as a Disease

CDG1m: Another name for Congenital disorder of glycosylation type 1M (or close medical condition association).
  »Introduction: Congenital disorder of glycosylation type 1M
  »Symptoms of Congenital disorder of glycosylation type 1M

CDG1m: Related Diseases

CDG1m: CDG1m 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 CDG1m (Congenital disorder of glycosylation type 1M)

Some of the symptoms of CDG1m incude:

• Retarded growth
• Small head
• Failure to thrive
• Retarded hair growth
• Seizures

See full list of 15 symptoms of CDG1m (Congenital disorder of glycosylation type 1M)

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Medical dictionaries:

• Medical dictionary,
• Medical Acronymns/Abbreviations

More Medical Dictionary Topics

Glycogen-Synthase-D Phosphatase

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