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VLINCL

Introduction: VLINCL

Description of VLINCL

VLINCL (medical condition): A rare metabolic disorder that affects the nerve cells of the body and is characterized by the deposits of lipopigments (lipofuscin). Type 5 is distinguished from other types by the origin of the genetic defect.

See also:

Ceroid lipofuscinosis, neuronal 5:
  »Introduction: Ceroid lipofuscinosis, neuronal 5
  »Symptoms of Ceroid lipofuscinosis, neuronal 5

VLINCL: Rare Disease

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

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

VLINCL as a Disease

VLINCL: Another name for Ceroid lipofuscinosis, neuronal 5 (or close medical condition association).
  »Introduction: Ceroid lipofuscinosis, neuronal 5
  »Symptoms of Ceroid lipofuscinosis, neuronal 5

Symptoms of VLINCL (Ceroid lipofuscinosis, neuronal 5)

Some of the symptoms of VLINCL incude:

Read more about symptoms of VLINCL (Ceroid lipofuscinosis, neuronal 5)

Terms associated with VLINCL:

Terms Similar to VLINCL:

Source - NIH

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