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Results 1 - 9 of 9 for Infertility disorder
  1. TSPYL1 gene 
    ... in the TSPYL1 gene associated 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
  2. FMR1 gene 
    ... irregular menstrual cycles, an inability to have children (infertility), early menopause, and elevated levels of a hormone ... FSH levels before age 40 and often causes infertility.For unknown reasons, the premutation leads to the ...
    https://medlineplus.gov/genetics/gene/fmr1 - Genetics
  3. NR5A1 gene 
    ... women, result in an inability to conceive children (infertility). AD4BP adrenal 4 binding protein ELP FTZ1 FTZF1 ... Seeler J, Achermann JC, McElreavey K. Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor ...
    https://medlineplus.gov/genetics/gene/nr5a1 - Genetics
  4. MED12 gene 
    ... lead to an inability to have biological children (infertility). Somatic MED12 gene mutations have also been identified ... article on PubMed Central Lyons MJ. MED12-Related Disorders. 2008 Jun 23 [updated 2021 Aug 12]. In: ...
    https://medlineplus.gov/genetics/gene/med12 - Genetics
  5. KAT6B gene 
    ... lead to an inability to have biological children (infertility). The genetic change associated with uterine leiomyomas is ... SP, Gibbs RA, Lee BH. The KAT6B-related disorders genitopatellar syndrome and Ohdo/SBBYS syndrome have distinct ...
    https://medlineplus.gov/genetics/gene/kat6b - Genetics
  6. CFTR gene 
    ... Cassiman JJ. CFTR mutations and polymorphisms in male infertility. Int J Androl. 2004 Oct;27(5):251- ... on PubMed Noone PG, Knowles MR. 'CFTR-opathies': disease phenotypes associated with cystic fibrosis transmembrane regulator gene ...
    https://medlineplus.gov/genetics/gene/cftr - Genetics
  7. FOXL2 gene 
    ... subfertility) or have a complete inability to conceive (infertility).The FOXL2 gene mutations that cause primary ovarian ... upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome. Am J Hum ...
    https://medlineplus.gov/genetics/gene/foxl2 - Genetics
  8. LHCGR gene 
    ... ovulation, leading to an inability to have children (infertility). FLJ41504 HHG LCGR LGR2 LH/CG-R LH/ ... OM, Chan WY. Luteinizing hormone receptor mutations in disorders of sexual development and cancer. Front Biosci. 2000 ...
    https://medlineplus.gov/genetics/gene/lhcgr - Genetics
  9. TBC1D20 gene 
    ... function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome ...
    https://medlineplus.gov/genetics/gene/tbc1d20 - Genetics