Find link

language:

jump to random article

Find link is a tool written by Edward Betts.

Longer titles found: Meesmann corneal dystrophy (view), Posterior polymorphous corneal dystrophy (view), Lattice corneal dystrophy (view), Macular corneal dystrophy (view), X-linked endothelial corneal dystrophy (view), Congenital stromal corneal dystrophy (view), Gelatinous drop-like corneal dystrophy (view), Granular corneal dystrophy (view), Reis–Bucklers corneal dystrophy (view), Fleck corneal dystrophy (view), Lisch epithelial corneal dystrophy (view), Subepithelial mucinous corneal dystrophy (view), Schnyder crystalline corneal dystrophy (view), Posterior amorphous corneal dystrophy (view), Spastic ataxia-corneal dystrophy syndrome (view)

searching for Corneal dystrophy 37 found (331 total)

alternate case: corneal dystrophy

Keratin 3 (221 words) [view diff] case mismatch in snippet view article find links to article

the KRT3 encoding this protein have been associated with Meesmanns Corneal Dystrophy. GRCh38: Ensembl release 89: ENSG00000186442 - Ensembl, May 2017 "Human
Corneodermatoosseous syndrome (106 words) [view diff] exact match in snippet view article find links to article
autosomal dominant condition with onset in infancy, characterized by corneal dystrophy, photophobia, diffuse palmoplantar keratoderma, distal onycholysis
Collagen, type VIII, alpha 2 (795 words) [view diff] exact match in snippet view article find links to article
positional candidate genes in patients with posterior polymorphous corneal dystrophy". Invest. Ophthalmol. Vis. Sci. 46 (5): 1599–603. doi:10.1167/iovs
Chromosome 5 (2,195 words) [view diff] exact match in snippet view article find links to article
Corneal dystrophy of Bowman layer Cri du chat Diastrophic dysplasia Ehlers-Danlos syndrome Familial adenomatous polyposis Granular corneal dystrophy type
Keratin disease (141 words) [view diff] exact match in snippet view article find links to article
skin KRT17 Monilethrix hair KRT81, KRT83, KRT86 Meesman juvenile epithelial corneal dystrophy cornea KRT3, KRT12 Familial cirrhosis liver KRT8, KRT18
ZEB1 (1,192 words) [view diff] exact match in snippet view article find links to article
right. Mutations of the gene are linked to posterior polymorphous corneal dystrophy 3. ZEB1 downregulates E-cadherin and induces epithelial to mesenchymal
Familial amyloid neuropathy (497 words) [view diff] exact match in snippet view article find links to article
"Amyloid". Akiya S, Nishio Y, Ibi K, et al. (July 1996). "Lattice corneal dystrophy type II associated with familial amyloid polyneuropathy type IV".
Nucleotide sugar (899 words) [view diff] exact match in snippet view article find links to article
resulted from altered function of UDP-GlcNAc epimerase . Macular corneal dystrophy: is a congenital disease resulted from malfunction of GlcNAc-6-sulfotransferase
List of diseases (K) (406 words) [view diff] exact match in snippet view article
cancer Keratosis palmoplantaris papulosa Keratosis palmoplantaris with corneal dystrophy Keratosis palmoplantar-periodontopathy Keratosis pilaris Keratosis
Collagen, type VIII, alpha 1 (756 words) [view diff] exact match in snippet view article find links to article
mutations identified in the COL8A1 and COL8A2 genes in familial Fuchs corneal dystrophy". Invest. Ophthalmol. Vis. Sci. 47 (9): 3787–90. doi:10.1167/iovs
Corneal abrasion (2,151 words) [view diff] exact match in snippet view article find links to article
recurrent feature in people who suffer specific types of corneal dystrophy, such as lattice corneal dystrophy. Lattice dystrophy gets its name from an accumulation
Krukenberg's spindle (192 words) [view diff] exact match in snippet view article find links to article
Maeda N, et al. (January 2000). "Corneal guttata associated with the corneal dystrophy resulting from a betaig-h3 R124H mutation". The British Journal of
CHST5 (485 words) [view diff] exact match in snippet view article find links to article
Shimomura Y, Kinoshita S, Tanigami A, Fukuda MN (Oct 2000). "Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase
Curly-coated Retriever (832 words) [view diff] exact match in snippet view article find links to article
Epilepsy Exercise-induced collapse Eye problems such as cataracts, corneal dystrophy, distichiasis, entropion, ectropion, or retinal dysplasia Gastric
Cavalier King Charles Spaniel (5,009 words) [view diff] exact match in snippet view article find links to article
Spaniels evaluated had eye problems. They include hereditary cataracts, corneal dystrophy, distichiasis, entropion, microphthalmia, progressive retinal atrophy
Sodium bicarbonate transporter-like protein 11 (765 words) [view diff] exact match in snippet view article find links to article
correlation and genetic analysis in a case of posterior polymorphous corneal dystrophy". Am. J. Ophthalmol. 135 (4): 461–70. CiteSeerX 10.1.1.582.4887. doi:10
Cairn Terrier (1,189 words) [view diff] exact match in snippet view article find links to article
problems found in the Cairn are: Bronchoesophageal fistula Cataracts Corneal dystrophy Craniomandibular osteopathy (lion jaw) Diabetes mellitus Entropion
List of diseases (L) (900 words) [view diff] exact match in snippet view article
dystrophy Lateral body wall defect Laterality defects dominant Lattice corneal dystrophy type 2 Launois–Bensaude adenolipomatosis Laurence–Prosser–Rocker syndrome
Ripasudil (1,215 words) [view diff] exact match in snippet view article find links to article
and therefore quick to reverse, unlike symptoms Fuchs endothelial corneal dystrophy, a disorder for which these short-lived symptoms could be mistaken
Maximilian Salzmann (338 words) [view diff] exact match in snippet view article find links to article
knötchenförmigen Hornhautdystrophie, 1925 – On a variety of tuberous corneal dystrophy. Glaukom und netzhautzirkulation, 1933 – Glaucoma and retinal circulation
CLK2 (944 words) [view diff] exact match in snippet view article find links to article
"Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p". American Journal of Human Genetics. 63 (4): 1073–7
Chromosome 10 (1,831 words) [view diff] exact match in snippet view article find links to article
dysplasia, Pakistani type Tetrahydrobiopterin deficiency Thiel–Behnke corneal dystrophy Usher syndrome Wolman syndrome Young-Simpson syndrome G-banding ideograms
Parson Russell Terrier (1,988 words) [view diff] exact match in snippet view article find links to article
conditions which appear in the breed include cataracts in juveniles, corneal dystrophy, progressive retinal atrophy and posterior vitreous detachment. Non-eye
King Charles Spaniel (5,223 words) [view diff] exact match in snippet view article find links to article
problems associated with the King Charles Spaniel include cataracts, corneal dystrophy, distichia, entropion, microphthalmia, optic disc drusen, and keratitis
King Charles Spaniel (5,223 words) [view diff] exact match in snippet view article find links to article
problems associated with the King Charles Spaniel include cataracts, corneal dystrophy, distichia, entropion, microphthalmia, optic disc drusen, and keratitis
Afghan Hound (3,089 words) [view diff] exact match in snippet view article find links to article
canthal pocket syndrome (breed predisposition due to shape of head), corneal dystrophy, cataract and generalized progressive retinal atrophy (GPRA). Afghan
Siberian Husky (3,916 words) [view diff] exact match in snippet view article find links to article
genetic, such as seizures and defects of the eye (juvenile cataracts, corneal dystrophy, canine glaucoma and progressive retinal atrophy) and congenital laryngeal
Golden Retriever (4,113 words) [view diff] exact match in snippet view article find links to article
with progressive retinal atrophy, glaucoma, distichiasis, entropion, corneal dystrophy, and retinal dysplasia. They may suffer from heart disease, especially
List of diseases (S) (1,928 words) [view diff] exact match in snippet view article
dysmorphism Spinocerebellar atrophy type 3 Spinocerebellar degeneration corneal dystrophy Spinocerebellar degenerescence book type Spirochetes disease Spirurida
Photorefractive keratectomy (2,772 words) [view diff] exact match in snippet view article find links to article
rheumatoid arthritis) History of side effects from steroids Granular corneal dystrophy type II Some complications that can be temporary or permanent include:
List of dog diseases (14,500 words) [view diff] exact match in snippet view article find links to article
spontaneously or with medical or surgical therapy. Corneal diseases Corneal dystrophy is a condition characterized by bilateral, noninflammatory opacity
Beagle (7,088 words) [view diff] exact match in snippet view article find links to article
problems; two common ophthalmic conditions in beagles are glaucoma and corneal dystrophy. "Cherry eye", a prolapse of the gland of the third eyelid, and distichiasis
Labrador Retriever (6,379 words) [view diff] exact match in snippet view article find links to article
some Labradors, particularly progressive retinal atrophy, cataracts, corneal dystrophy and retinal dysplasia. Dogs which are intended to be bred should be
Collagen (6,848 words) [view diff] exact match in snippet view article find links to article
VIII Some endothelial cells COL8A1, COL8A2 Posterior polymorphous corneal dystrophy 2 IX FACIT collagen, cartilage, assoc. with type II and XI fibrils
Carbohydrate sulfotransferase (2,073 words) [view diff] case mismatch in snippet view article find links to article
Carbohydrate sulfotransferases 6 (CHST6) is associated with Macular Corneal Dystrophy (MCD) Inheritance: Autosomal recessive. Genetic Locus: 16q22 Online
Contact lens (9,460 words) [view diff] exact match in snippet view article find links to article
corneal edema, descemetocele, corneal ectasia, Mooren's ulcer, anterior corneal dystrophy, and neurotrophic keratoconjunctivitis. Contact lenses that deliver
Human genome (10,960 words) [view diff] exact match in snippet view article find links to article
mention are Kallman syndrome and Pfeiffer syndrome (gene FGFR1), Fuchs corneal dystrophy (gene TCF4), Hirschsprung's disease (genes RET and FECH), Bardet-Biedl