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Dictionary » Congenital Oculomotor Apraxia
 

Congenital Oculomotor Apraxia

Introduction: Congenital Oculomotor Apraxia

Description of Congenital Oculomotor Apraxia

Congenital Oculomotor Apraxia (medical condition): A rare inherited condition where the person is unable to move eyes...more »

See also:

Apraxia, oculomotor, Cogan type:
  »Introduction: Apraxia, oculomotor, Cogan type
  »Symptoms of Apraxia, oculomotor, Cogan type

Congenital Oculomotor Apraxia: Related Topics

These medical condition or symptom topics may be relevant to medical information for Congenital Oculomotor Apraxia:

Congenital Oculomotor Apraxia: Rare Disease

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

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

Congenital Oculomotor Apraxia as a Disease

Congenital Oculomotor Apraxia: Another name for Apraxia, oculomotor, Cogan type (or close medical condition association).
  »Introduction: Apraxia, oculomotor, Cogan type
  »Symptoms of Apraxia, oculomotor, Cogan type

Congenital Oculomotor Apraxia: Related Diseases

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

Symptoms of Congenital Oculomotor Apraxia (Apraxia, oculomotor, Cogan type)

Some of the symptoms of Congenital Oculomotor Apraxia incude:

Congenital Oculomotor Apraxia: Related Disease Topics

These medical disease topics may be related to Congenital Oculomotor Apraxia:

Terms associated with Congenital Oculomotor Apraxia:

Terms Similar to Congenital Oculomotor Apraxia:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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