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Dictionary » Congenital atransferrinemia (subtype)
 

Congenital atransferrinemia (subtype)

Introduction: Congenital atransferrinemia (subtype)

Description of Congenital atransferrinemia (subtype)

Congenital atransferrinemia (subtype) (medical condition): A rare inherited condition characterized by the absence of a compound...more »

See also:

Atransferrinemia:
  »Introduction: Atransferrinemia
  »Symptoms of Atransferrinemia

Congenital atransferrinemia (subtype): Related Topics

These medical condition or symptom topics may be relevant to medical information for Congenital atransferrinemia (subtype):

Congenital atransferrinemia (subtype): Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Congenital atransferrinemia (subtype) is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Congenital atransferrinemia (subtype), or a subtype of Congenital atransferrinemia (subtype), affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Congenital atransferrinemia (subtype) as a Disease

Congenital atransferrinemia (subtype): Another name for Atransferrinemia (or close medical condition association).
  »Introduction: Atransferrinemia
  »Symptoms of Atransferrinemia

Congenital atransferrinemia (subtype): Related Diseases

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

Symptoms of Congenital atransferrinemia (subtype) (Atransferrinemia)

Some of the symptoms of Congenital atransferrinemia (subtype) incude:

Congenital atransferrinemia (subtype): Related Disease Topics

These medical disease topics may be related to Congenital atransferrinemia (subtype):

Terms associated with Congenital atransferrinemia (subtype):

Terms Similar to Congenital atransferrinemia (subtype):

Source - NIH

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