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Dictionary » Familial LSA (type)
 

Familial LSA (type)

Familial LSA (type): Related Topics

These medical condition or symptom topics may be relevant to medical information for Familial LSA (type):

Familial LSA (type): Rare Disease

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

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

Terms associated with Familial LSA (type):

Terms Similar to Familial LSA (type):

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

  • Synovitis granulomatous uveitis cranial neuropathies
  • Synovitis granulomatous with uveitis and cranial neuropathies
  • Synovitis sicca
  • Synovitis, Acne, Pustlosis, Hyperostosis, and Osteomyelitis
  • Synovitis, acne, pustulosis, hyperostosis, osteomyelitis
  • Synovitis, Pigmented Villonodular
  • Synovium
  • Synpolydactyly
  • Synpolydactyly 1
  • SYNS2
  • Synsepalum
  • Synspondylism

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