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Results 1 - 10 of 19 for albino
  1. Oculocutaneous albinism 
    Oculocutaneous albinism is a group of conditions that affect coloring (pigmentation) of the skin, hair, and eyes. Affected individuals typically have very fair skin ...
    https://medlineplus.gov/genetics/condition/oculocutaneous-albinism - Genetics
  2. Ocular albinism 
    Ocular albinism is a genetic condition that primarily affects the eyes. This condition reduces the coloring (pigmentation) of the iris, which is the colored ...
    https://medlineplus.gov/genetics/condition/ocular-albinism - Genetics
  3. Tietz syndrome 
    ... affected person has one parent with the condition. Albinism and complete nerve deafness Albinism-deafness of Tietz Hypopigmentation-deafness syndrome Hypopigmentation/deafness ...
    https://medlineplus.gov/genetics/condition/tietz-syndrome - Genetics
  4. OCA2 gene 
    ... of people with Angelman syndrome also have oculocutaneous albinism type 2. This condition occurs when people have ... of melanin, leading to the characteristic features of albinism. More About This Health Condition More than 80 ...
    https://medlineplus.gov/genetics/gene/oca2 - Genetics
  5. GPR143 gene 
    ... people with the most common form of ocular albinism, which is called the Nettleship-Falls type or ... and other eye abnormalities in people with ocular albinism.Most forms of albinism result from a reduced ...
    https://medlineplus.gov/genetics/gene/gpr143 - Genetics
  6. Griscelli syndrome 
    ... of the condition. GS Hypopigmentation immunodeficiency disease Partial albinism with immunodeficiency Genetic Testing Registry: Griscelli syndrome type ...
    https://medlineplus.gov/genetics/condition/griscelli-syndrome - Genetics
  7. Hermansky-Pudlak syndrome 
    ... a disorder characterized by a condition called oculocutaneous albinism, which causes abnormally light coloring (pigmentation) of the ... cancers caused by long-term sun exposure. Oculocutaneous albinism reduces pigmentation of the colored part of the ...
    https://medlineplus.gov/genetics/condition/hermansky-pudlak-syndrome - Genetics
  8. Chediak-Higashi syndrome 
    ... is also characterized by a condition called oculocutaneous albinism, which causes abnormally light coloring (pigmentation) of the ... colored hair, often with a metallic sheen. Oculocutaneous albinism also causes vision problems such as reduced sharpness; ...
    https://medlineplus.gov/genetics/condition/chediak-higashi-syndrome - Genetics
  9. TYR gene 
    ... gene have been identified in people with oculocutaneous albinism type 1. These mutations disrupt the normal production ... life. These mutations cause a form of oculocutaneous albinism called type 1A (OCA1A). People with this form ...
    https://medlineplus.gov/genetics/gene/tyr - Genetics
  10. TYRP1 gene 
    ... TYRP1 gene have been found to cause oculocutaneous albinism type 3. This condition includes a form of albinism called rufous oculocutaneous albinism, which has been described ...
    https://medlineplus.gov/genetics/gene/tyrp1 - Genetics
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