Home Page
References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 15-07-2010
Symbol RS
Location 1q42.12
Name Reynolds syndrome
Other name(s) primary biliary cirrhosis, scleroderma, Raynaud disease, and telangiectasia
Corresponding gene LBR
related resource Retinal Information Network
Main clinical features
  • liver disease like pruritis, jaundice, hepatomegaly
  • telangiectasia, Raynaud phenomenon, and variable features of scleroderma
  • Genetic determination
    Function/system disorder
    Type disease
    Remark(s)