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Results 1 - 10 of 19 for Gonadal "dysgenesis," male
  1. Noonan syndrome 
    ... cause the disorder. Familial Turner syndrome Female pseudo-Turner syndrome Male Turner syndrome Noonan's syndrome Noonan-Ehmke syndrome NS Pseudo- ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  2. Denys-Drash syndrome 
    ... typical male chromosome pattern (46,XY), they have gonadal dysgenesis, in which external genitalia do not look clearly male or clearly female or the genitalia appear female- ...
    https://medlineplus.gov/genetics/condition/denys-drash-syndrome - Genetics
  3. Frasier syndrome 
    ... typical male chromosome pattern (46,XY), they have gonadal dysgenesis, in which external genitalia do not look clearly male or clearly female or the genitalia appear female- ...
    https://medlineplus.gov/genetics/condition/frasier-syndrome - Genetics
  4. NR5A1 gene 
    ... disorder of sex development, also known as partial gonadal dysgenesis. Affected individuals may have external genitalia that do not look clearly male-typical or clearly female-typical or other abnormalities ...
    https://medlineplus.gov/genetics/gene/nr5a1 - Genetics
  5. SRY gene 
    ... XY complete gonadal dysgenesis or 46,XY pure gonadal dysgenesis. Swyer syndrome is a condition that affects sex development. Individual with this condition have a male-typical chromosome pattern (46,XY karyotype), but they ...
    https://medlineplus.gov/genetics/gene/sry - Genetics
  6. DHH gene 
    ... disorder of sex development, also known as partial gonadal dysgenesis. These individuals have one altered DHH gene in each cell. They may have external genitalia that do not look clearly male or clearly female or other changes in the ...
    https://medlineplus.gov/genetics/gene/dhh - Genetics
  7. MAP3K1 gene 
    ... sex development, which is also known as partial gonadal dysgenesis. These ... do not look clearly male or clearly female or other abnormalities of the ...
    https://medlineplus.gov/genetics/gene/map3k1 - Genetics
  8. Turner syndrome 
    ... cell: generally, females have two X chromosomes, while males have one X chromosome and one Y chromosome. Turner syndrome results when one normal X chromosome is present ...
    https://medlineplus.gov/genetics/condition/turner-syndrome - Genetics
  9. Perrault syndrome 
    ... not show signs and symptoms of the condition. Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance Gonadal dysgenesis with sensorineural deafness, autosomal recessive inheritance Gonadal dysgenesis, ...
    https://medlineplus.gov/genetics/condition/perrault-syndrome - Genetics
  10. X chromosome 
    ... BH, Visootsak J, Brady AN, Graham JM Jr. Turner syndrome: an update and review ... evaluation of 46,XX males and review of the literature. J Pediatr Endocrinol ...
    https://medlineplus.gov/genetics/chromosome/x - Genetics
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