Concept information
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Pigmentation Disorders
Hypopigmentation
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Skin Diseases, Genetic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Preferred term
Albinism
Type
-
Topical Descriptor
Broader concept
Narrower concepts
Note
- general or unspecified; prefer specifics
Scope note
- General term for a number of inherited defects of amino acid metabolism in which there is a deficiency or absence of pigment in the eyes, skin, or hair.
In other languages
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Finnish
-
albiino
-
albiinous
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albinism
-
albinismus
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Chediak-Steinbrinck-Higashin oireyhtymä
-
Chediak-Steinbrinck-Higashin syndrooma
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Chediak-Steinbrinck-Higashis syndrom
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Cross syndrom
-
Crossin oireyhtymä
-
Crossin syndrooma
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Hermansky-Pudlakin oireyhtymä
-
Hermansky-Pudlakin syndrooma
-
Hermansky-Pudlaks syndrom
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syndroma Chediak-Steinbrinck-Higashi
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syndroma Cross
-
syndroma Hermansky-Pudlak
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syndroma Waardenburg
-
Waardenburg syndrom
-
Waardenburgin oireyhtymä
-
Waardenburgin syndrooma
-
Swedish
URI
http://www.yso.fi/onto/mesh/D000417
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