CDG 1D

Introduction: CDG 1D

Description of CDG 1D

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

See also:

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

CDG 1D: Related Topics

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

• CDG
• CDG syndrome

CDG 1D as a Disease

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

CDG 1D: Related Diseases

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

Some of the symptoms of CDG 1D incude:

• Psychomotor retardation
• Hypotonia
• Seizures
• Optic atrophy
• Small head

See full list of 7 symptoms of CDG 1D (Congenital disorder of glycosylation type 1D)

CDG 1D: Related Disease Topics

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

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

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Medical dictionaries:

• Medical dictionary,
• Medical Acronymns/Abbreviations

More Medical Dictionary Topics

Sphenoid

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