アッシャー症候群
1. Usher syndromeUsher syndrome (sometimes referred to as "Usher's syndrome") is a relatively rare genetic disorder that is a leading cause of deafblindness and that is associated with a mutation in any one of 10 genes. Other names for Usher syndrome include Hallgren syndrome, Usher-Hallgren syndrome, rp-dysacusis syndrome and dystrophia retinae dysacusis syndrome.
Read “Usher syndrome” on English Wikipedia
Read “アッシャー症候群” on Japanese Wikipedia
Read “Usher syndrome” on DBpedia
Read “Usher syndrome” on English Wikipedia
Read “アッシャー症候群” on Japanese Wikipedia
Read “Usher syndrome” on DBpedia
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