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Results 1 - 10 of 25 for Usher syndrome type 2
  1. Usher syndrome 
    ... Registry: Usher syndrome type 1F Genetic Testing Registry: Usher syndrome type 2 Usher syndrome National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
    https://medlineplus.gov/genetics/condition/usher-syndrome - Genetics
  2. Usher Syndrome From the National Institutes of Health (National Institute on Deafness and Other Communication Disorders)  
    Usher Syndrome/Learn More ... Usher Syndrome ... National Institute on Deafness and Other Communication Disorders ... From the National Institutes of Health ... Usher syndrome ...
    https://www.nidcd.nih.gov/health/usher-syndrome - External Health Links
  3. MYO7A gene 
    ... Zhao C. Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2. PLoS One. 2014 May 15;9(5):e97808. ... et al. Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature. 1995 Mar 2;374(6517):60-1. doi: 10.1038/374060a0. ...
    https://medlineplus.gov/genetics/gene/myo7a - Genetics
  4. CLRN1 gene 
    ... protein leads to the signs and symptoms of Usher syndrome type IIIA.Two particular CLRN1 gene mutations are most common in ...
    https://medlineplus.gov/genetics/gene/clrn1 - Genetics
  5. Facts about Usher Syndrome From the National Institutes of Health (National Eye Institute)  
    Usher Syndrome/Learn More ... Usher Syndrome ... National Eye Institute ... From the National Institutes of Health ... Usher syndrome is the most common condition that affects ...
    https://www.nei.nih.gov/.../usher-syndrome - External Health Links
  6. USH2A gene 
    ... novel basement membrane protein defective in people with Usher's syndrome type IIa. Hear Res. 2002 Jan;163(1-2):1-11. doi: 10.1016/s0378-5955(01)00344-6. Citation on PubMed Blanco-Kelly F, Jaijo T, Aller E, ... Ayuso C. Clinical aspects of Usher syndrome and the USH2A gene in a cohort of ...
    https://medlineplus.gov/genetics/gene/ush2a - Genetics
  7. CDH23 gene 
    ... deafness. Am J Hum Genet. 2002 Aug;71(2):262-75. doi: 10.1086/341558. Epub 2002 ... gene family, causes Usher syndrome type 1D. Nat Genet. 2001 Jan;27(1):108- ...
    https://medlineplus.gov/genetics/gene/cdh23 - Genetics
  8. 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
  9. Usher Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Usher Syndrome/Learn More ... Usher Syndrome ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and other information ...
    https://rarediseases.info.nih.gov/diseases/7843/usher-syndrome - External Health Links
  10. Benign Paroxysmal Positional Vertigo (BPPV) (Vestibular Disorders Association)  
    Dizziness and Vertigo/Specifics ... Dizziness and Vertigo ... Vestibular Disorders Association ... Benign Paroxysmal Positional Vertigo (BPPV) is the most common cause ...
    https://vestibular.org/.../benign-paroxysmal-positional-vertigo-bppv - External Health Links
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