Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 28 for Male pseudohermaphroditism
  1. 5-alpha reductase deficiency 
    ... reductase type 2 gene (SRD5A2) leads to severe male pseudohermaphroditism in a Turkish family. Urology. 2005 Aug;66( ...
    https://medlineplus.gov/.../condition/5-alpha-reductase-deficiency - Genetics
  2. Partial androgen insensitivity syndrome 
    Partial androgen insensitivity syndrome (PAIS) is when a person who has one X and one Y chromosome (typically seen in males) but is ...
    https://medlineplus.gov/ency/article/001169.htm - Medical Encyclopedia
  3. Persistent Müllerian duct syndrome 
    Persistent Müllerian duct syndrome is a disorder of sexual development that affects males. Males with this disorder have normal male reproductive organs, though ...
    https://medlineplus.gov/.../persistent-mullerian-duct-syndrome - Genetics
  4. Leydig cell hypoplasia 
    ... the luteinizing hormone/chorionic gonadotropin receptor gene cause male pseudohermaphroditism. PLoS Med. 2008 Apr 22;5(4):e88. ... with a novel missense mutation of LHCGR cause male pseudohermaphroditism. Hum Mutat. 2009 Sep;30(9):E855-65. ...
    https://medlineplus.gov/genetics/condition/leydig-cell-hypoplasia - Genetics
  5. LHCGR gene 
    ... the luteinizing hormone/chorionic gonadotropin receptor gene cause male pseudohermaphroditism. PLoS Med. 2008 Apr 22;5(4):e88. ... with a novel missense mutation of LHCGR cause male pseudohermaphroditism. Hum Mutat. 2009 Sep;30(9):E855-65. ...
    https://medlineplus.gov/genetics/gene/lhcgr - Genetics
  6. Campomelic dysplasia From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Birth Defects/Specifics ... Birth Defects ... Bone Diseases/Children ... Bone Diseases ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health
    https://rarediseases.info.nih.gov/.../10027/campomelic-dysplasia - External Health Links
  7. 17-beta hydroxysteroid dehydrogenase 3 deficiency 
    ... KSR deficiency Neutral 17-beta-hydroxysteroid oxidoreductase deficiency Pseudohermaphroditism, male, with gynecomastia Testosterone 17-beta-dehydrogenase deficiency 46, ...
    https://medlineplus.gov/...hydroxysteroid-dehydrogenase-3-deficiency - Genetics
  8. 46,XX testicular difference of sex development 
    ... XX testicular disorder/difference of sex development XX male syndrome Genetic Testing Registry: 46,XX testicular disorder of sex development 46,XX testicular disorder of sex development National ...
    https://medlineplus.gov/...-testicular-difference-of-sex-development - Genetics
  9. TSPYL1 gene 
    ... in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility. Fertil Steril. 2009 Oct;92(4):1347- ...
    https://medlineplus.gov/genetics/gene/tspyl1 - Genetics
  10. DHH gene 
    ... have external genitalia that do not look clearly male or clearly female or other changes in the genitals and reproductive organs.Some people with the features of 46,XY disorder of sex development caused by DHH gene variants also have nerve ...
    https://medlineplus.gov/genetics/gene/dhh - Genetics
previous · 1 · 2 · 3 · next