CDG 1E

Introduction: CDG 1E

Description of CDG 1E

CDG 1E (medical condition): A very rare inherited metabolic disorder where...more »

See also:

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

CDG 1E: Related Topics

These medical condition or symptom topics may be relevant to medical information for CDG 1E:

• CDG
• CDG syndrome

CDG 1E as a Disease

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

CDG 1E: Related Diseases

CDG 1E: CDG 1E 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 CDG 1E (Congenital disorder of glycosylation type 1E)

Some of the symptoms of CDG 1E incude:

• Dysmorphic features
• Psychomotor retardation
• Hypotonia
• Seizures
• Cortical blindness

See full list of 9 symptoms of CDG 1E (Congenital disorder of glycosylation type 1E)

CDG 1E: Related Disease Topics

These medical disease topics may be related to CDG 1E:

• inherited metabolic disorder
• psychomotor retardation
• hypotonia
• seizures
• liver disease

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Medical dictionaries:

• Medical dictionary,
• Medical Acronymns/Abbreviations

More Medical Dictionary Topics

Microcephaly seizures mental retardation heart disease

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