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BFIC1

Introduction: BFIC1

Description of BFIC1

BFIC1 (medical condition): An inherited form of seizures that occurs in infancy and early...more »

See also:

Convulsions, benign familial infantile, 1:
  »Introduction: Convulsions, benign familial infantile, 1
  »Symptoms of Convulsions, benign familial infantile, 1

BFIC1: Rare Disease

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

BFIC1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that BFIC1, or a subtype of BFIC1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

BFIC1 as a Disease

BFIC1: Another name for Convulsions, benign familial infantile, 1 (or close medical condition association).
  »Introduction: Convulsions, benign familial infantile, 1
  »Symptoms of Convulsions, benign familial infantile, 1

BFIC1: Related Diseases

BFIC1: BFIC1 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of BFIC1 (Convulsions, benign familial infantile, 1)

Some of the symptoms of BFIC1 incude:

Terms associated with BFIC1:

Terms Similar to BFIC1:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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