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GENATLAS PHENOTYPE
last update : 4/09/2006
Symbol ODG1
Location 2p16
Name ovarian dysgenesis, XX type
Other name(s) gonadal dysgenesis XX
Corresponding gene FSHR
Other symbol(s) XXGD, GDXX
Main clinical features
  • ovarian dysgenesis, hypergonadotropic
  • primary amenorrhea
  • normal stature
  • primary ovarian failure
    • Genetic determination autosomal recessive
    Function/system disorder endocrinology
    Type disease
    Gene product
    Name follicle stimulating hormone receptor (FSHR)
    Remark(s)