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GENATLAS PHENOTYPE
last update : 23-03-2021
Symbol POF9
Location 1p22.2
Name premature ovarian failure 9
Corresponding gene HFM1
Main clinical features
  • nonsyndromic primary ovarian insufficiency, which is characterized by amenorrhea with elevated gonadotropin levels
  • Genetic determination autosomal recessive
    Function/system disorder sex-genitalia
    Type disease
    Remark(s)