Joint Shantou International Eye Centre of Shantou University and The Chinese University of Hong Kong

By gene
  
By phenotype
  



Gene : FBLN5
    
OMIM : 604580
    
UniProt : Q9UBX5
    
AmiGO : Q9UBX5
    
Phenotype : Macular degeneration, age-related, 3 Neuropathy, hereditary, with or without age-related macular degeneration Cutis laxa, autosomal domit 2 Charcot-Marie-Tooth disease, demyelinating, type 1H Cutis laxa, autosomal recessive, type IA