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Results 1 - 10 of 26 for "Deafness," autosomal recessive 9
  1. Nonsyndromic hearing loss 
    ... RECESSIVE 2; DFNB2 DEAFNESS, AUTOSOMAL DOMINANT 4A; DFNA4A DEAFNESS, AUTOSOMAL RECESSIVE 9; DFNB9 DEAFNESS, AUTOSOMAL RECESSIVE 1A; DFNB1A DEAFNESS, AUTOSOMAL ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  2. GJB3 gene 
    ... on PubMed Petersen MB, Willems PJ. Non-syndromic, autosomal-recessive ... Dec;20(4):366-9. doi: 10.1038/3840. Citation on PubMed Scott ...
    https://medlineplus.gov/genetics/gene/gjb3 - Genetics
  3. STRC gene 
    ... in affected males. More About This Health Condition deafness, autosomal recessive 16 DFNB16 STRC_HUMAN Tests of STRC PubMed ...
    https://medlineplus.gov/genetics/gene/strc - Genetics
  4. TECTA gene 
    ... alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21. Hum Mol Genet. 1999 Mar;8(3): ...
    https://medlineplus.gov/genetics/gene/tecta - Genetics
  5. SLC26A4 gene 
    The SLC26A4 gene provides instructions for making a protein called pendrin. This protein transports negatively charged particles (ions), including chloride, ...
    https://medlineplus.gov/genetics/gene/slc26a4 - Genetics
  6. Keratitis-ichthyosis-deafness syndrome 
    ... dominant keratitis-ichthyosis-hearing loss syndrome Keratitis-ichthyosis-deafness syndrome, autosomal recessive KID syndrome National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/.../keratitis-ichthyosis-deafness-syndrome - Genetics
  7. MYO7A gene 
    ... F, Drira M, Ayadi H, Petit C. The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic ...
    https://medlineplus.gov/genetics/gene/myo7a - Genetics
  8. Sensorineural deafness and male infertility 
    ... and male infertility. CATSPER2 STRC chromosome 15 Sensorineural deafness and male infertility is inherited in an autosomal recessive pattern, which means both copies of chromosome 15 ...
    https://medlineplus.gov/...nsorineural-deafness-and-male-infertility - Genetics
  9. Charcot-Marie-Tooth disease 
    ... MOTOR AND SENSORY, WITH EXCESSIVE MYELIN FOLDING COMPLEX, AUTOSOMAL RECESSIVE NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH DEAFNESS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND ABSENT SENSORY LARGE MYELINATED ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  10. Pendred syndrome 
    ... not show signs and symptoms of the condition. Autosomal recessive sensorineural hearing impairment, enlarged vestibular aqueduct, and goiter Deafness with goiter Goiter-deafness syndrome Pendred's syndrome ...
    https://medlineplus.gov/genetics/condition/pendred-syndrome - Genetics
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