ONKI3 | Medical Subject Headings

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Corneal Dystrophies, Hereditary

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Eye Diseases, Hereditary ∟ Corneal Dystrophies, Hereditary 15 coordinate concepts 2 subordinate concepts ∟ Corneal Dystrophy, Juvenile Epithelial of Meesmann \| ∟ Fuchs' Endothelial Dystrophy ∟ Corneal Edema \| ∟ Corneal Neovascularization \| ∟ Corneal Opacity \| ∟ Keratitis \| ∟ Keratoconus \| ∟ Trachoma \| ∟ Albinism \| ∟ Aniridia \| ∟ Choroideremia \| ∟ Duane Retraction Syndrome \| ∟ Graves Ophthalmopathy \| ∟ Gyrate Atrophy \| ∟ Optic Atrophies, Hereditary \| ∟ Retinal Dysplasia \| ∟ Retinitis Pigmentosa Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Corneal Diseases ∟ Corneal Dystrophies, Hereditary 15 coordinate concepts 2 subordinate concepts ∟ Corneal Dystrophy, Juvenile Epithelial of Meesmann \| ∟ Fuchs' Endothelial Dystrophy ∟ Corneal Edema \| ∟ Corneal Neovascularization \| ∟ Corneal Opacity \| ∟ Keratitis \| ∟ Keratoconus \| ∟ Trachoma \| ∟ Albinism \| ∟ Aniridia \| ∟ Choroideremia \| ∟ Duane Retraction Syndrome \| ∟ Graves Ophthalmopathy \| ∟ Gyrate Atrophy \| ∟ Optic Atrophies, Hereditary \| ∟ Retinal Dysplasia \| ∟ Retinitis Pigmentosa Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Eye Diseases, Hereditary ∟ Corneal Dystrophies, Hereditary 15 coordinate concepts 2 subordinate concepts ∟ Corneal Dystrophy, Juvenile Epithelial of Meesmann \| ∟ Fuchs' Endothelial Dystrophy ∟ Corneal Edema \| ∟ Corneal Neovascularization \| ∟ Corneal Opacity \| ∟ Keratitis \| ∟ Keratoconus \| ∟ Trachoma \| ∟ Albinism \| ∟ Aniridia \| ∟ Choroideremia \| ∟ Duane Retraction Syndrome \| ∟ Graves Ophthalmopathy \| ∟ Gyrate Atrophy \| ∟ Optic Atrophies, Hereditary \| ∟ Retinal Dysplasia \| ∟ Retinitis Pigmentosa X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Eye Diseases, Hereditary ∟ Corneal Dystrophies, Hereditary Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Corneal Diseases ∟ Corneal Dystrophies, Hereditary Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Eye Diseases, Hereditary ∟ Corneal Dystrophies, Hereditary Eye Diseases, Hereditary > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Corneal Diseases > Eye Diseases > Medical Subject Headings (MeSH) Eye Diseases, Hereditary > Eye Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Corneal Dystrophy, Juvenile Epithelial of Meesmann \| Fuchs' Endothelial Dystrophy X
historyNote*:	90; was CORNEAL DYSTROPHIES 1963-89 X
onlineNote*:	use CORNEAL DYSTROPHIES, HEREDITARY to search CORNEAL DYSTROPHIES 1966-89 X
publicMeSHNote*:	90; was CORNEAL DYSTROPHIES 1963-89 X
Scope note:	Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect. X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Corneal Edema \| Corneal Neovascularization \| Corneal Opacity \| Keratitis \| Keratoconus \| Trachoma \| Albinism \| Aniridia \| Choroideremia \| Duane Retraction Syndrome \| Graves Ophthalmopathy \| Gyrate Atrophy \| Optic Atrophies, Hereditary \| Retinal Dysplasia \| Retinitis Pigmentosa X
URI:	X
Labels and equivalent concepts:	Perinnölliset sarveiskalvorappeumat (fi) Täpläinen sarveiskalvorappeuma (fi, replaced) Verkkomainen sarveiskalvorappeuma (fi, replaced) Periytyvät sarveiskalvodystrofiat (fi, replaced) Periytyvät korneadystrofiat (fi, replaced) Periytyvä sarveiskalvodystrofia (fi, replaced) Periytyvä korneadystrofia (fi, replaced) Perinnölliset sarveiskalvon rappeumat (fi, replaced) Jyväinen sarveiskalvorappeuma (fi, replaced) Hereditaariset sarveiskalvodystrofiat (fi, replaced) Hereditaariset korneadystrofiat (fi, replaced) Fuchsin rappeuma (fi, replaced) Perinnöllinen korneadystrofia (fi, replaced) Perinnöllinen sarveiskalvodystrofia (fi, replaced) Perinnölliset sarveiskalvodystrofiat (fi, replaced) Perinnölliset korneadystrofiat (fi, replaced) Perinnöllinen sarveiskalvorappeuma (fi, replaced) Perinnöllinen sarveiskalvon rappeuma (fi, replaced) Epiteliaalinen sarveiskalvorappeuma (fi, replaced) Hornhinnedystrofier, ärftliga (sv) Korneadystrofier, ärftliga (sv, replaced) Dystrophia corneae epithelialis (la-FI, replaced) Dystrophia corneae granularis (la-FI, replaced) Dystrophia Fuchs (la-FI, replaced) Dystrophia corneae macularis (la-FI, replaced) Dystrophia corneae hereditaria (la-FI, replaced) X
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