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USH1C

Introduction: USH1C

Description of USH1C

USH1C (medical condition): A rare inherited disorder characterized by sensorineural deafness and...more »

See also:

Usher syndrome, type 1C:
  »Introduction: Usher syndrome, type 1C
  »Symptoms of Usher syndrome, type 1C

USH1C: Related Topics

These medical condition or symptom topics may be relevant to medical information for USH1C:

USH1C: Rare Disease

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

USH1C is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that USH1C, or a subtype of USH1C, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

USH1C as a Disease

USH1C: Another name for Usher syndrome, type 1C (or close medical condition association).
  »Introduction: Usher syndrome, type 1C
  »Symptoms of Usher syndrome, type 1C

USH1C: Related Diseases

USH1C: USH1C is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of USH1C (Usher syndrome, type 1C)

Some of the symptoms of USH1C incude:

USH1C: Related Disease Topics

These medical disease topics may be related to USH1C:

Terms associated with USH1C:

Terms Similar to USH1C:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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