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Results 1 - 5 of 5 for Usher "syndrome," type 2A
  1. Usher syndrome 
    ... Registry: Usher syndrome type 1K Genetic Testing Registry: Usher syndrome type 2A Genetic Testing Registry: Usher syndrome type 2C Genetic Testing Registry: Usher syndrome type 2D ...
    https://medlineplus.gov/genetics/condition/usher-syndrome - Genetics
  2. USH2A gene 
    ... H. Identification of 51 novel exons of the Usher syndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type II. Am J Hum Genet. 2004 Apr;74( ...
    https://medlineplus.gov/genetics/gene/ush2a - Genetics
  3. Retinitis Pigmentosa (Foundation Fighting Blindness)  
    Retinal Disorders/Specifics ... Retinal Disorders ... Usher Syndrome/Learn More ... Usher Syndrome ... Foundation Fighting Blindness ... What is Retinitis Pigmentosa? Learn about ...
    https://www.fightingblindness.org/diseases/retinitis-pigmentosa - External Health Links
  4. Bardet-Biedl Syndrome (Foundation Fighting Blindness)  
    Retinal Disorders/Specifics ... Retinal Disorders ... Birth Defects/Specifics ... Birth Defects ... Foundation Fighting Blindness ... What is Bardet Biedl Syndrome? Learn about ...
    https://www.fightingblindness.org/diseases/bardet-biedl-syndrome-bbs - External Health Links
  5. Nonsyndromic hearing loss 
    ... cause syndromic forms of hearing loss, such as Usher syndrome (CDH23 and MYO7A, among others), Pendred syndrome (SLC26A4), ... DEAFNESS, AUTOSOMAL DOMINANT 3A; DFNA3A DEAFNESS, AUTOSOMAL DOMINANT 2A; DFNA2A DEAFNESS, X-LINKED 3; DFNX3 DEAFNESS, AUTOSOMAL ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics