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Results 1 - 7 of 7 for Cochlear disorder
  1. COL4A5 gene 
    ... on PubMed Kashtan CE. Alport syndrome. An inherited disorder of renal, ocular, and cochlear basement membranes. Medicine (Baltimore). 1999 Sep;78(5): ...
    https://medlineplus.gov/genetics/gene/col4a5 - Genetics
  2. COL4A4 gene 
    ... on PubMed Kashtan CE. Alport syndrome. An inherited disorder of renal, ocular, and cochlear basement membranes. Medicine (Baltimore). 1999 Sep;78(5): ...
    https://medlineplus.gov/genetics/gene/col4a4 - Genetics
  3. Deafness and myopia syndrome 
    ... symptoms of the condition. Deafness and myopia Deafness, cochlear, plus DFNMYP High myopia and ... PubMed Aruga J, ...
    https://medlineplus.gov/.../condition/deafness-and-myopia-syndrome - Genetics
  4. Sialidosis 
    ... Vacuolization and alterations of lysosomal membrane proteins in cochlear marginal ... article on PubMed Central
    https://medlineplus.gov/genetics/condition/sialidosis - Genetics
  5. NEU1 gene 
    ... build up inside lysosomes are called lysosomal storage disorders. Mutations that eliminate NEU1 enzyme ... membrane proteins in cochlear marginal cells contribute to hearing loss in neuraminidase ...
    https://medlineplus.gov/genetics/gene/neu1 - Genetics
  6. MITF gene 
    ... for Identifying Pathophysiology and Therapeutic Approach of Pigmentary ... Tachibana M. Cochlear melanocytes and MITF signaling. J Investig Dermatol Symp ...
    https://medlineplus.gov/genetics/gene/mitf - Genetics
  7. USH2A gene 
    ... USH2A gene mutations cause a form of the disorder known as Usher syndrome type IIA (USH2A), which ... photoreceptors and normal development of cochlear hair cells. Proc Natl Acad Sci U S ...
    https://medlineplus.gov/genetics/gene/ush2a - Genetics