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Medical Subject Headings

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Sisällön kieli

Käsitteen tiedot

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

Käytettävä termi

Leber Congenital Amaurosis  

Tyyppi

  • Topical Descriptor

Yläkäsite

Ohjaustermit

  • 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

Käyttöhuomautus

  • 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.

Huomautus muutoshistoriasta

  • 2010

Muunkieliset termit

URI

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

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RDF/XML TURTLE JSON-LD Luotu 6.7.2009, viimeksi muokattu 11.4.2022