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, Ocular

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Eye Diseases, Hereditary ∟ Albinism ∟ Albinism, Ocular 2 coordinate concepts ∟ Albinism, Oculocutaneous \| ∟ 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, Ocular 2 coordinate concepts ∟ Albinism, Oculocutaneous \| ∟ Piebaldism Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Albinism ∟ Albinism, Ocular 2 coordinate concepts ∟ Albinism, Oculocutaneous \| ∟ Piebaldism Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Eye Diseases, Hereditary ∟ Albinism ∟ Albinism, Ocular 2 coordinate concepts ∟ Albinism, Oculocutaneous \| ∟ Piebaldism Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Amino Acid Metabolism, Inborn Errors ∟ Albinism ∟ Albinism, Ocular 2 coordinate concepts ∟ Albinism, Oculocutaneous \| ∟ Piebaldism Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Pigmentation Disorders ∟ Hypopigmentation ∟ Albinism ∟ Albinism, Ocular 2 coordinate concepts ∟ Albinism, Oculocutaneous \| ∟ Piebaldism Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Albinism ∟ Albinism, Ocular 2 coordinate concepts ∟ Albinism, Oculocutaneous \| ∟ Piebaldism X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Eye Diseases, Hereditary ∟ Albinism ∟ Albinism, Ocular Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Amino Acid Metabolism, Inborn Errors ∟ Albinism ∟ Albinism, Ocular Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Albinism ∟ Albinism, Ocular Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Eye Diseases, Hereditary ∟ Albinism ∟ Albinism, Ocular Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Amino Acid Metabolism, Inborn Errors ∟ Albinism ∟ Albinism, Ocular Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Pigmentation Disorders ∟ Hypopigmentation ∟ Albinism ∟ Albinism, Ocular Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Albinism ∟ Albinism, Ocular 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
Annotation:	hypopigmentation of eye; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES X
History note:	Albinism (1966-1990)X
historyNote*:	91 X
publicMeSHNote*:	91 X
Scope note:	Albinism affecting the eye in which pigment of the hair and skin is normal or only slightly diluted. The classic type is X-linked (Nettleship-Falls), but an autosomal recessive form also exists. Ocular abnormalities may include reduced pigmentation of the iris, nystagmus, photophobia, strabismus, and decreased visual acuity. 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, Oculocutaneous \| Piebaldism X
URI:	X
Labels and equivalent concepts:	Silmän albinismi (fi) Silmän albiinous (fi, replaced) Okulaarinen albinismi (fi, replaced) Forsius-Eriksonin tauti (fi, replaced) Okulaarinen albiinous (fi, replaced) Ahvenanmaan silmätauti (fi, replaced) Albinism, okulär (sv) Okulär albinism (sv, replaced) Albinismus ocularis (la-FI, replaced) X
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