(Q55780357)

English

helicoid peripapillary chorioretinal degeneration

An eye disease characterized by presence in the fundus of progressive bilateral retinal and choroidal atrophy leading to central vision loss that has material basis in heterozygous muation in TEAD1 on 11p15.3.

  • SVEINSSON CHORIORETINAL ATROPHY; SCRA
  • atrophia areata
  • Peripapillary Chorioretinal Degeneration, Icelandic Type
  • SVEINSSON CHORIORETINAL ATROPHY
  • SCRA
  • HPCD
  • Helicoidal Peripapillary Chorioretinal Degeneration
  • peripapillary chorioretinal degeneration, Icelandic type
  • Sveinsson chorioretinal atrophy
  • Atrophia Areata

Statements

Identifiers

 
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