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type
seeAlso
sameAs
notation
  • C11.768.585.865
alternative label
  • Juvenile Retinoschises
  • Juvenile Retinoschisis, X-Linked
  • Retinoschises, X-Linked
  • Retinoschisis, X-Linked Juvenile
  • Juvenile Retinoschises, X-Linked
  • Juvenile Retinoschisis
  • Retinoschisis, X-Linked
  • X Linked Retinoschisis
  • X-Linked Juvenile Retinoschisis
  • X-Linked Retinoschises
  • X-Linked Retinoschisis
  • Congenital X-Linked Retinoschisis
  • Retinoschisis
  • Retinoschisis X-Linked Juvenile
  • Retinoschisis, Juvenile, X-Linked
  • Retinoschisis, X Linked
  • Rétinoschisis dégénératif
  • Rétinoschisis juvénile lié à l'X
  • X Linked Juvenile Retinoschisis
  • Degenerative Retinoschises
  • Degenerative Retinoschisis
  • Retinoschises, Degenerative
  • Retinoschises, Juvenile
  • Retinoschises, X-Linked Juvenile
  • Retinoschisis, Degenerative
  • Retinoschisis, Juvenile
  • Retinoschisis, Juvenile, X Chromosome-Linked
  • X-Linked Juvenile Retinoschises
  • Retinoschises
  • Congenital X Linked Retinoschisis
  • Congenital X-Linked Retinoschises
  • Retinoschises, Congenital X-Linked
  • Retinoschisis, Congenital X-Linked
  • X-Linked Retinoschises, Congenital
  • X-Linked Retinoschisis, Congenital
preferred label
  • Rétinoschisis
is in scheme
note
  • Splitting of the RETINA into two layers at the level of the outer plexiform layer, beginning as a cystic degeneration in the extreme retinal periphery. It usually occurs after 40 years of age and is generally not progressive
  • A vitreoretinal dystrophy characterized by splitting of the neuroretinal layers. It occurs in two forms: degenerative retinoschisis and X chromosome-linked juvenile retinoschisis
  • X chromosome recessive disorder, found nearly exclusively in males and becoming apparent around puberty. Characterized initially by a cystlike structure involving the FOVEA CENTRALIS, a peripheral retinoschisis occurs in about half the patients
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