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Begreppsinformation

Eye Diseases > Retinal Diseases > Leber Congenital Amaurosis
Eye Diseases > Eye Diseases, Hereditary > Leber Congenital Amaurosis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Eye Diseases, Hereditary > Leber Congenital Amaurosis

Föredragen term

Leber Congenital Amaurosis  

Typ

  • Topical Descriptor

Överordnat begrepp

Hänvisningstermer

  • Abiotrophies, Leber
  • Abiotrophy, Leber
  • Amauroses, Leber's
  • Amaurosis, Leber Congenital
  • Amaurosis, Leber's
  • Blindness, Congenital Retinal
  • Blindnesses, Congenital Retinal
  • Congenital Retinal Blindness
  • Congenital Retinal Blindnesses
  • Leber Abiotrophies
  • Leber Abiotrophy
  • Leber Amaurosis
  • Leber Congenital Tapetoretinal Degeneration
  • Leber's Amauroses
  • Leber's Amaurosis
  • Lebers Amaurosis
  • Retinal Blindnesses, Congenital

Användningsanmärkning

  • A rare degenerative inherited eye disease that appears at birth or in the first few months of life that results in a loss of vision. Not to be confused with LEBER HEREDITARY OPTIC NEUROPATHY, the disease is thought to be caused by abnormal development of PHOTORECEPTOR CELLS in the RETINA, or by the extremely premature degeneration of retinal cells.

Anmärkning om ändringshistoria

  • 2010

Termer på andra språk

URI

http://www.yso.fi/onto/mesh/D057130

Ladda ned detta begrepp:

RDF/XML TURTLE JSON-LD Skapad 2009-07-06, senast editerad 2022-04-11