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Results 1 - 3 of 3 for MYO7A
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  1. Usher syndrome 
    ... type I. The most common of these are MYO7A gene mutations, followed by mutations in the CDH23 ... are probably associated with this disorder. CDH23 CLRN1 MYO7A USH2A Additional Information from NCBI Gene: ADGRV1 CIB2 ...
    https://medlineplus.gov/genetics/condition/usher-syndrome - Genetics
  2. Nonsyndromic hearing loss 
    ... hearing loss, such as Usher syndrome (CDH23 and MYO7A, among others), Pendred syndrome (SLC26A4), Wolfram syndrome (WFS1), ... DSPP GJB2 GJB3 GJB6 KCNQ4 MT-TS1 MYH9 MYO7A POU3F4 PRPS1 SLC26A4 STRC TBC1D24 TECTA WFS1 mitochondrial ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  3. Age-related hearing loss 
    ... and hearing is unclear. APOE CDH23 KCNQ4 MTHFR MYO7A SLC26A4 mitochondrial dna Additional Information from NCBI Gene: ...
    https://medlineplus.gov/genetics/condition/age-related-hearing-loss - Genetics