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 - 5 of 5 for Ovarian dysgenesis
  1. HSD17B4 gene 
    ... Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome. Am ...
    https://medlineplus.gov/genetics/gene/hsd17b4 - Genetics
  2. HARS2 gene 
    ... Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome. Proc ...
    https://medlineplus.gov/genetics/gene/hars2 - Genetics
  3. NR5A1 gene 
    ... K, Bashamboo A. Mutations in NR5A1 associated with ovarian insufficiency. N ... Morel Y. Gonadal dysgenesis without adrenal insufficiency in a 46, XY patient ...
    https://medlineplus.gov/genetics/gene/nr5a1 - Genetics
  4. SRY gene 
    ... syndrome, also known as 46,XY complete gonadal dysgenesis or 46,XY pure gonadal dysgenesis. Swyer syndrome is a condition that affects sex ... XY difference of sex development, or partial gonadal dysgenesis. The effects of these variants on the function ...
    https://medlineplus.gov/genetics/gene/sry - Genetics
  5. WNT4 gene 
    ... MEMBER 4; WNT4 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS; SERKAL NCBI Gene ... and adult ovaries and its signaling contributes to ovarian cell survival. Mol Cell Endocrinol. 2010 Apr 12; ...
    https://medlineplus.gov/genetics/gene/wnt4 - Genetics