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Results 1 - 10 of 23 for Kallmann syndrome 1
  1. Kallmann syndrome 
    Kallmann syndrome is a condition characterized by delayed or absent puberty and an impaired sense of smell.This disorder is a form of hypogonadotropic hypogonadism, ...
    https://medlineplus.gov/genetics/condition/kallmann-syndrome - Genetics
  2. ANOS1 gene 
    ... ANOS1 gene have been identified in people with Kallmann syndrome, a disorder characterized by the combination of hypogonadotropic ... 5 to 10 percent of all cases of Kallmann syndrome.The ANOS1 gene mutations that cause Kallmann syndrome ...
    https://medlineplus.gov/genetics/gene/anos1 - Genetics
  3. PROKR2 gene 
    ... 30 mutations in the PROKR2 gene can cause Kallmann syndrome, a disorder characterized by the combination of hypogonadotropic ... for about 9 percent of all cases of Kallmann syndrome.Most of the PROKR2 gene mutations that cause ...
    https://medlineplus.gov/genetics/gene/prokr2 - Genetics
  4. FGFR1 gene 
    ... than 140 FGFR1 gene mutations that can cause Kallmann syndrome, a disorder characterized by the combination of hypogonadotropic ... for about 10 percent of all cases of Kallmann syndrome.The FGFR1 gene mutations that cause Kallmann syndrome ...
    https://medlineplus.gov/genetics/gene/fgfr1 - Genetics
  5. CHD7 gene 
    ... CHD7 gene have been identified in people with Kallmann syndrome, a disorder characterized by the combination of hypogonadotropic ... 5 to 10 percent of all cases of Kallmann syndrome.Many people with Kallmann syndrome caused by a ...
    https://medlineplus.gov/genetics/gene/chd7 - Genetics
  6. PROK2 gene 
    ... PROK2 gene have been identified in people with Kallmann syndrome, a disorder characterized by the combination of hypogonadotropic ... for about 9 percent of all cases of Kallmann syndrome.Most of the PROK2 gene mutations that cause ...
    https://medlineplus.gov/genetics/gene/prok2 - Genetics
  7. FGF8 gene 
    ... FGF8 gene have been identified in people with Kallmann syndrome, a disorder characterized by the combination of hypogonadotropic ... for a small percentage of all cases of Kallmann syndrome.Most of the FGF8 gene mutations that cause ...
    https://medlineplus.gov/genetics/gene/fgf8 - Genetics
  8. Male Hypogonadism (Mayo Foundation for Medical Education and Research)  
    Sexual Problems in Men/Related Issues ... Sexual Problems in Men ... Endocrine Diseases/Men ... Endocrine Diseases ... Mayo Foundation for Medical Education and Research
    https://www.mayoclinic.org/.../symptoms-causes/syc-20354881?p=1 - External Health Links
  9. Hypogonadism 
    ... Tumors A genetic cause of central hypogonadism is Kallmann syndrome . Many people with this condition also have a ...
    https://medlineplus.gov/ency/article/001195.htm - Medical Encyclopedia
  10. Endocrine Diseases (National Library of Medicine)  
    Your endocrine system includes eight major glands throughout your body. These glands make hormones. Hormones are chemical messengers. They travel through ...
    https://medlineplus.gov/endocrinediseases.html - Health Topics
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