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Results 1 - 10 of 11 for Male Infertility
  1. CATSPER1 gene 
    ... have been found to cause CATSPER1-related nonsyndromic male infertility. These mutations are thought to lead to the ... are the cause of infertility in affected males. Male infertility is the only symptom of CATSPER1-related nonsyndromic ...
    https://medlineplus.gov/genetics/gene/catsper1 - Genetics
  2. CATSPER2 gene 
    ... during fertilization. The symptoms of sensorineural deafness and male infertility are caused by a deletion of genetic material ... D, Beckmann JS. CATSPER2, a human autosomal nonsyndromic male infertility gene. Eur J Hum Genet. 2003 Jul;11( ...
    https://medlineplus.gov/genetics/gene/catsper2 - Genetics
  3. STRC gene 
    ... More About This Health Condition Sensorineural deafness and male infertility is a condition caused by a deletion of ... A, Najmabadi H, Smith RJ. Sensorineural deafness and male infertility: a contiguous gene deletion syndrome. J Med Genet. ...
    https://medlineplus.gov/genetics/gene/strc - Genetics
  4. TSPYL1 gene 
    ... with 46,XY disorder of sex development and male infertility. Fertil Steril. 2009 Oct;92(4):1347-1350. ...
    https://medlineplus.gov/genetics/gene/tspyl1 - Genetics
  5. AURKC gene 
    ... AURKC yields large-headed polyploid spermatozoa and causes male infertility. Nat Genet. 2007 May;39(5):661-5. ...
    https://medlineplus.gov/genetics/gene/aurkc - Genetics
  6. CFTR gene 
    ... H, Cassiman JJ. CFTR mutations and polymorphisms in male infertility. Int J Androl. 2004 Oct;27(5):251- ...
    https://medlineplus.gov/genetics/gene/cftr - Genetics
  7. TBC1D20 gene 
    ... of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome ...
    https://medlineplus.gov/genetics/gene/tbc1d20 - Genetics
  8. NR5A1 gene 
    ... C, Seeler J, Achermann JC, McElreavey K. Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor ...
    https://medlineplus.gov/genetics/gene/nr5a1 - Genetics
  9. DCXR gene 
    ... lack of symptoms in people with essential pentosuria.Males with essential pentosuria appear ... carbonyl reductase 2 ...
    https://medlineplus.gov/genetics/gene/dcxr - Genetics
  10. LHCGR gene 
    ... gene mutations that cause Leydig cell hypoplasia in males have normal female genitalia and ... FLJ41504 HHG LCGR LGR2 LH/CG-R LH/ ...
    https://medlineplus.gov/genetics/gene/lhcgr - Genetics
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