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SCKL1

Introduction: SCKL1

Description of SCKL1

SCKL1 (medical condition): Seckel syndrome is a rare inherited disorder mainly...more »

See also:

Seckel syndrome 1:
  »Introduction: Seckel syndrome 1
  »Symptoms of Seckel syndrome 1

SCKL1: Rare Disease

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

SCKL1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that SCKL1, or a subtype of SCKL1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

SCKL1 as a Disease

SCKL1: Another name for Seckel syndrome 1 (or close medical condition association).
  »Introduction: Seckel syndrome 1
  »Symptoms of Seckel syndrome 1

SCKL1: Related Diseases

SCKL1: SCKL1 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of SCKL1 (Seckel syndrome 1)

Some of the symptoms of SCKL1 incude:

Terms associated with SCKL1:

Terms Similar to SCKL1:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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