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References OMIM Gene GeneReviews HGMD HGNC
last update : 02-04-2019
Symbol AA
Location 11p15.3
HGNC id 11
Name atrophia areata
Other name(s)
  • Sveinsson chorioretinal atrophy
  • helicoid peripapillary chorioretinal degeneration
  • Corresponding gene TEAD1
    related resource Retinal Information Network
    Other symbol(s) SCRA
    Main clinical features
  • icelandic type, symmetrical lesions radiating from the optic disc, involving retina and choroid
  • Genetic determination autosomal dominant
    Function/system disorder eye
    Type disease
    Gene product
    Name TEA domain family member 1
    Remark(s) . mutation has been shown previously to disrupt the YAP1-TEAD interaction (Jianzhong 2010)