ONKI3 | Medical Subject Headings

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Corneal Dystrophy, Juvenile Epithelial of Meesmann

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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 ∟ Corneal Dystrophy, Juvenile Epithelial of Meesmann 1 coordinate concept ∟ Fuchs' Endothelial Dystrophy Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Corneal Diseases ∟ Corneal Dystrophies, Hereditary ∟ Corneal Dystrophy, Juvenile Epithelial of Meesmann 1 coordinate concept ∟ Fuchs' Endothelial Dystrophy Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Eye Diseases, Hereditary ∟ Corneal Dystrophies, Hereditary ∟ Corneal Dystrophy, Juvenile Epithelial of Meesmann 1 coordinate concept ∟ Fuchs' Endothelial Dystrophy X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Eye Diseases, Hereditary ∟ Corneal Dystrophies, Hereditary ∟ Corneal Dystrophy, Juvenile Epithelial of Meesmann Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Corneal Diseases ∟ Corneal Dystrophies, Hereditary ∟ Corneal Dystrophy, Juvenile Epithelial of Meesmann Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Eye Diseases, Hereditary ∟ Corneal Dystrophies, Hereditary ∟ Corneal Dystrophy, Juvenile Epithelial of Meesmann Corneal Dystrophies, Hereditary > Eye Diseases, Hereditary > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Corneal Dystrophies, Hereditary > Corneal Diseases > Eye Diseases > Medical Subject Headings (MeSH) Corneal Dystrophies, Hereditary > Eye Diseases, Hereditary > Eye Diseases > Medical Subject Headings (MeSH) X
History note:	Cornea (1954-1964) \| Corneal Dystrophies, Hereditary (1965-2006)X
historyNote*:	2007 X
publicMeSHNote*:	2007 X
Scope note:	An autosomal dominant form of hereditary corneal dystrophy due to a defect in cornea-specific KERATIN formation. Mutations in the genes that encode KERATIN-3 and KERATIN-12 have been linked to this disorder. X
activeMeSHYear*:	2007X
dateCreated*:	2006-07-05X
dateEstablished*:	2007-01-01X
recordAuthorizer*:	sjnX
recordMaintainer*:	jmpX
recordOriginator*:	jmpX
Type:	Concept X
Coordinate terms:	Fuchs' Endothelial Dystrophy X
URI:	X
Labels and equivalent concepts:	Meesmannin lasten epiteliaalinen sarveiskalvon dystrofia (fi) Meesmann Corneal Epithelial Dystrophy (en, replaced) X
Share:	X