ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Albinism, Oculocutaneous

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Eye Diseases, Hereditary ∟ Albinism ∟ Albinism, Oculocutaneous 2 coordinate concepts 1 subordinate concept ∟ Hermanski-Pudlak Syndrome ∟ Albinism, Ocular \| ∟ Piebaldism Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Amino Acid Metabolism, Inborn Errors ∟ Albinism ∟ Albinism, Oculocutaneous 2 coordinate concepts 1 subordinate concept ∟ Hermanski-Pudlak Syndrome ∟ Albinism, Ocular \| ∟ Piebaldism Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Albinism ∟ Albinism, Oculocutaneous 2 coordinate concepts 1 subordinate concept ∟ Hermanski-Pudlak Syndrome ∟ Albinism, Ocular \| ∟ Piebaldism Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Eye Diseases, Hereditary ∟ Albinism ∟ Albinism, Oculocutaneous 2 coordinate concepts 1 subordinate concept ∟ Hermanski-Pudlak Syndrome ∟ Albinism, Ocular \| ∟ Piebaldism Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Amino Acid Metabolism, Inborn Errors ∟ Albinism ∟ Albinism, Oculocutaneous 2 coordinate concepts 1 subordinate concept ∟ Hermanski-Pudlak Syndrome ∟ Albinism, Ocular \| ∟ Piebaldism Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Pigmentation Disorders ∟ Hypopigmentation ∟ Albinism ∟ Albinism, Oculocutaneous 2 coordinate concepts 1 subordinate concept ∟ Hermanski-Pudlak Syndrome ∟ Albinism, Ocular \| ∟ Piebaldism Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Albinism ∟ Albinism, Oculocutaneous 2 coordinate concepts 1 subordinate concept ∟ Hermanski-Pudlak Syndrome ∟ Albinism, Ocular \| ∟ Piebaldism X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Eye Diseases, Hereditary ∟ Albinism ∟ Albinism, Oculocutaneous Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Amino Acid Metabolism, Inborn Errors ∟ Albinism ∟ Albinism, Oculocutaneous Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Albinism ∟ Albinism, Oculocutaneous Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Eye Diseases, Hereditary ∟ Albinism ∟ Albinism, Oculocutaneous Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Amino Acid Metabolism, Inborn Errors ∟ Albinism ∟ Albinism, Oculocutaneous Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Pigmentation Disorders ∟ Hypopigmentation ∟ Albinism ∟ Albinism, Oculocutaneous Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Albinism ∟ Albinism, Oculocutaneous Albinism > Eye Diseases, Hereditary > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Albinism > Amino Acid Metabolism, Inborn Errors > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Albinism > Skin Diseases, Genetic > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Albinism > Eye Diseases, Hereditary > Eye Diseases > Medical Subject Headings (MeSH) Albinism > Amino Acid Metabolism, Inborn Errors > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Albinism > Hypopigmentation > Pigmentation Disorders > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) Albinism > Skin Diseases, Genetic > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Hermanski-Pudlak Syndrome X
History note:	Albinism (1966-1990)X
historyNote*:	91 X
publicMeSHNote*:	91 X
Scope note:	Heterogeneous group of autosomal recessive disorders comprising at least four recognized types, all having in common varying degrees of hypopigmentation of the skin, hair, and eyes. The two most common are the tyrosinase-positive and tyrosinase-negative types. X
activeMeSHYear*:	2007X
dateCreated*:	1990-02-12X
dateEstablished*:	1991-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	AGSX
Type:	Concept X
Coordinate terms:	Albinism, Ocular \| Piebaldism X
URI:	X
Labels and equivalent concepts:	Silmän ja ihon albinismi (fi) Silmän ja ihon albiinous (fi, replaced) Okulokutaaninen albinismi (fi, replaced) Okulokutaaninen albiinous (fi, replaced) Albinism, okulokutan (sv) Okulokutan albinism (sv, replaced) Albinismus oculocutaneus (la-FI, replaced) X
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