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ETM1

Introduction: ETM1

Description of ETM1

ETM1 (medical condition): An inherited movement disorder involving tremors...more »

See also:

Tremor hereditary essential, 1:
  »Introduction: Tremor hereditary essential, 1
  »Symptoms of Tremor hereditary essential, 1

ETM1: Rare Disease

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

ETM1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that ETM1, or a subtype of ETM1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

ETM1 as a Disease

ETM1: Another name for Tremor hereditary essential, 1 (or close medical condition association).
  »Introduction: Tremor hereditary essential, 1
  »Symptoms of Tremor hereditary essential, 1

ETM1: Related Diseases

ETM1: ETM1 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of ETM1 (Tremor hereditary essential, 1)

Some of the symptoms of ETM1 incude:

ETM1: Related Disease Topics

These medical disease topics may be related to ETM1:

Terms associated with ETM1:

Terms Similar to ETM1:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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