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40 relations: Cholesterol, CHST6, Collagen, type VIII, alpha 2, Congenital hereditary endothelial dystrophy, Congenital stromal corneal dystrophy, Cornea, Corneal dystrophies in dogs, Corneal transplantation, Decorin, Epithelial basement membrane dystrophy, Fleck corneal dystrophy, Fuchs' dystrophy, Gelatinous drop-like corneal dystrophy, Gelsolin, Granular corneal dystrophy, Keratin 12, Keratin 3, Keratoconus, Keratoglobus, Lattice corneal dystrophy, Lipid, Lisch epithelial corneal dystrophy, Macular corneal dystrophy, Meesmann corneal dystrophy, Ophthalmology, Orphanet Journal of Rare Diseases, PIKFYVE, Posterior polymorphous corneal dystrophy, Recurrent corneal erosion, Reis–Bucklers corneal dystrophy, Schnyder crystalline corneal dystrophy, SLC4A11, Subepithelial mucinous corneal dystrophy, TACSTD2, TGFBI, Thiel–Behnke dystrophy, UBIAD1, X-linked endothelial corneal dystrophy, X-linked reticulate pigmentary disorder, ZEB1.
Cholesterol
Cholesterol (from the Ancient Greek chole- (bile) and stereos (solid), followed by the chemical suffix -ol for an alcohol) is an organic molecule.
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CHST6
Carbohydrate sulfotransferase 6 is an enzyme that in humans is encoded by the CHST6 gene.
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Collagen, type VIII, alpha 2
Collagen alpha-2(VIII) chain is a protein that in humans is encoded by the COL8A2 gene.
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Congenital hereditary endothelial dystrophy
Congenital hereditary corneal dystrophy (CHED) is a form of corneal dystrophy which presents at birth.
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Congenital stromal corneal dystrophy
Congenital stromal corneal dystrophy (CSCD), also called Witschel dystrophy, is an extremely rare, autosomal dominant form of corneal dystrophy.
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Cornea
The cornea is the transparent front part of the eye that covers the iris, pupil, and anterior chamber.
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Corneal dystrophies in dogs
Corneal dystrophies are a group of diseases that affect the cornea in dogs.
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Corneal transplantation
Corneal transplantation, also known as corneal grafting, is a surgical procedure where a damaged or diseased cornea is replaced by donated corneal tissue (the graft).
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Decorin
Decorin is a protein that in humans is encoded by the DCN gene.
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Epithelial basement membrane dystrophy
Epithelial basement membrane dystrophy (EBMD), also known as map-dot-fingerprint dystrophy and Cogans's microcystic dystrophy, is a disorder of the eye that can cause pain and dryness.
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Fleck corneal dystrophy
Fleck corneal dystrophy, also known as Francois-Neetens speckled corneal dystrophy, is a rare form of corneal dystrophy.
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Fuchs' dystrophy
Fuchs' dystrophy, also referred to as Fuchs' corneal endothelial dystrophy (FCED) and Fuchs' endothelial dystrophy (FED), is a slowly progressing corneal dystrophy that usually affects both eyes and is slightly more common in women than in men.
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Gelatinous drop-like corneal dystrophy
Gelatinous drop-like corneal dystrophy, also known as amyloid corneal dystrophy, is a rare form of corneal dystrophy.
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Gelsolin
Gelsolin is an actin-binding protein that is a key regulator of actin filament assembly and disassembly.
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Granular corneal dystrophy
Granular corneal dystrophy is a slowly progressive corneal dystrophy that most often begins in early childhood.
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Keratin 12
Keratin 12 is a protein that in humans is encoded by the KRT12 gene.
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Keratin 3
Keratin 3 also known as cytokeratin 3 is a protein that in humans is encoded by the KRT3 gene.
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Keratoconus
Keratoconus (KC) is a disorder of the eye which results in progressive thinning of the cornea.
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Keratoglobus
Keratoglobus (from Greek: kerato- horn, cornea; and Latin: globus round), is a degenerative non-inflammatory disorder of the eye in which structural changes within the cornea cause it to become extremely thin and change to a more globular shape than its normal gradual curve.
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Lattice corneal dystrophy
Lattice corneal dystrophy type, also known as Biber-Haab-Dimmer dystrophy, is a rare form of corneal dystrophy.
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Lipid
In biology and biochemistry, a lipid is a biomolecule that is soluble in nonpolar solvents.
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Lisch epithelial corneal dystrophy
Lisch epithelial corneal dystrophy (LECD), also known as band-shaped and whorled microcystic dystrophy of the corneal epithelium, is a rare form of corneal dystrophy first described in 1992 by Lisch et al.
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Macular corneal dystrophy
Macular corneal dystrophy, also known as Fehr corneal dystrophy named for German ophthalmologist Oskar Fehr (1871-1959), is a rare pathological condition affecting the stroma of cornea.
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Meesmann corneal dystrophy
Meesmann corneal dystrophy, also Stocker-Holt dystrophy, is a type of corneal dystrophy and a keratin disease.
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Ophthalmology
Ophthalmology is a branch of medicine and surgery (both methods are used) that deals with the anatomy, physiology and diseases of the eyeball and orbit.
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Orphanet Journal of Rare Diseases
The Orphanet Journal of Rare Diseases is a peer-reviewed open access medical journal covering research on rare diseases.
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PIKFYVE
PIKfyve, a FYVE finger-containing phosphoinositide kinase, is an enzyme that in humans is encoded by the PIKFYVE gene.
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Posterior polymorphous corneal dystrophy
Posterior Polymorphous Corneal Dystrophy (PPCD; sometimes also Schlichting dystrophy) is a type of corneal dystrophy, characterised by changes in Descemet's membrane and endothelial layer.
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Recurrent corneal erosion
Recurrent corneal erosion is a disorder of the eyes characterized by the failure of the cornea's outermost layer of epithelial cells to attach to the underlying basement membrane (Bowman's layer).
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Reis–Bucklers corneal dystrophy
Reis-Bücklers corneal dystrophy, also known as corneal dystrophy of Bowman layer, type I, is a rare, corneal dystrophy of unknown cause, in which the Bowman's layer of the cornea undergoes disintegration.
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Schnyder crystalline corneal dystrophy
Schnyder crystalline corneal dystrophy (SCD) is a rare form of corneal dystrophy.
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SLC4A11
Sodium bicarbonate transporter-like protein 11 is a protein that in humans is encoded by the SLC4A11 gene.
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Subepithelial mucinous corneal dystrophy
Subepithelial mucinous corneal dystrophy (SMCD) is a rare form of corneal dystrophy.
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TACSTD2
Tumor-associated calcium signal transducer 2, also known as Trop-2 and as epithelial glycoprotein-1 antigen (EGP-1), is a protein that in humans is encoded by the TACSTD2 gene.
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TGFBI
Transforming growth factor, beta-induced, 68kDa, also known as TGFBI (initially called BIGH3, BIG-H3), is a protein which in humans is encoded by the TGFBI gene, locus 5q31.
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Thiel–Behnke dystrophy
Thiel–Behnke dystrophy, or Corneal dystrophy of Bowman layer, type II, is a rare form of corneal dystrophy affecting the layer that supports corneal epithelium.
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UBIAD1
UbiA prenyltransferase domain-containing protein 1 (UBIAD1) also known as transitional epithelial response protein 1 (TERE1) is a protein that in humans is encoded by the UBIAD1 gene.
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X-linked endothelial corneal dystrophy
X-linked endothelial corneal dystrophy (XECD) is a rare form of corneal dystrophy described first in 2006, based on a 4-generation family of 60 members with 9 affected males and 35 trait carriers, which led to mapping the XECD locus to Xq25.
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X-linked reticulate pigmentary disorder
X-linked reticulate pigmentary disorder (also known as "familial cutaneous amyloidosis", "Partington amyloidosis", "Partington cutaneous amyloidosis", "Partington syndrome type II", "reticulate pigmentary disorder", and "X-linked reticulate pigmentary disorder with systemic manifestations") is a cutaneous condition that has been described in adult women that had linear streaks of hyperpigmentation and in which male patients manifested a reticulated mottled brown pigmentation of the skin, which, on biopsy, demonstrated dermal deposits of amyloid.
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ZEB1
Zinc finger E-box-binding homeobox 1 is a protein that in humans is encoded by the ZEB1 gene.
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Redirects here:
Corneal dystrophies in human, Corneal dystrophies in humans, Corneal dystrophy (human), Familial corneal amyloidosis, Hereditary corneal dystrophies, Hereditary corneal dystrophy.
References
[1] https://en.wikipedia.org/wiki/Corneal_dystrophy
