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Results 1 - 9 of 9 for Kallmann syndrome 3
  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 
    ... FGFR1 gene variants have been found to cause Kallmann syndrome, a disorder characterized by the combination of hypogonadotropic ... for about 10 percent of all cases of Kallmann syndrome. The FGFR1 gene variants 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. 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
  7. 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
  8. SOX10 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Kallmann syndrome More About This Health Condition DOM dominant megacolon, ...
    https://medlineplus.gov/genetics/gene/sox10 - Genetics
  9. Congenital fibrosis of the extraocular muscles 
    ... vocal cords; and a set of symptoms called Kallmann syndrome, which features delayed or absent puberty and an ...
    https://medlineplus.gov/...nital-fibrosis-of-the-extraocular-muscles - Genetics