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Results 1 - 10 of 35 for "Deafness," autosomal recessive 6
  1. ... DEAFNESS, X-LINKED 1; DFNX1 DEAFNESS, AUTOSOMAL DOMINANT 6; DFNA6 DEAFNESS, X-LINKED 5, WITH PERIPHERAL NEUROPATHY; DFNX5 DEAFNESS, AUTOSOMAL RECESSIVE 7; DFNB7 DEAFNESS, X-LINKED 4; DFNX4 DEAFNESS, ...
  2. ... dysfunction, autosomal recessive inheritance Gonadal dysgenesis with sensorineural deafness, autosomal recessive inheritance Gonadal dysgenesis, XX type, with deafness Ovarian ...
  3. ... in affected males. More About This Health Condition deafness, autosomal recessive 16 DFNB16 STRC_HUMAN Tests of STRC PubMed ...
  4. ... 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): ...
  5. The SLC26A4 gene provides instructions for making a protein called pendrin. This protein transports negatively charged particles (ions), including chloride, ...
  6. ... type 1b Renal tubular acidosis with progressive nerve deafness Renal tubular acidosis, autosomal recessive, with progressive nerve deafness Renal tubular acidosis, distal, ...
  7. ... type chloride channel accessory beta subunit BSND_HUMAN deafness, autosomal recessive 73 DFNB73 Tests of BSND PubMed BARTTIN CLCNK- ...
  8. ... TB, Morell RJ. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the ...
  9. ... F, Drira M, Ayadi H, Petit C. The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic ...
  10. ... MYOPIA 13, X-LINKED; MYP13 MYOPIA 18, AUTOSOMAL RECESSIVE; MYP18 MYOPIA 3, AUTOSOMAL DOMINANT; MYP3 MYOPIA 6; MYP6 MYOPIA 17, AUTOSOMAL DOMINANT; MYP17 MYOPIA 5, ...
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