Corneal Dystrophies, Hereditary [dědičné dystrofie rohovky]

topical
63
Terms

dystrofie rohovky - dědičná
granulární dystrofie rohovky
Groenouwův typ dystrofie rohovky
makulární dystrofie rohovky
rohovka - dystrofie dědičné
stromální dystrofie rohovky

 

Corneal Dystrophies
Granular Dystrophy, Corneal
Groenouw's Dystrophies
Macular Dystrophy, Corneal
Stromal Dystrophies, Corneal

Persistent link   https://www.medvik.cz/link/D003317
Definition

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.

DUI
D003317 MeSH Browser
CUI
M0005178
History note
90; was CORNEAL DYSTROPHIES 1963-89
Online note
use CORNEAL DYSTROPHIES, HEREDITARY to search CORNEAL DYSTROPHIES 1966-89
Public note
90; was CORNEAL DYSTROPHIES 1963-89

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 9
CO
complications 2
DI
diagnosis 18
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology 3
EH
ethnology
ET
etiology 5
GE
genetics 33
HI
history
IM
immunology 1
ME
metabolism 7
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 21
PP
physiopathology 3
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery 4
TH
therapy 5
UR
urine
VE
veterinary
VI
virology

C Diseases
C11 Eye Diseases 1 489
C11.204 Corneal Diseases 253
C11.204.236 Corneal Dystrophies, Hereditary 63
C11.204.236.218 Corneal Dystrophy, Juvenile Epithelial of Meesmann 1
C11.204.236.438 Fuchs' Endothelial Dystrophy 15
C11.204.267 Corneal Edema 16
C11.204.278 Corneal Endothelial Cell Loss 11
C11.204.284 Corneal Injuries 60
C11.204.290 Corneal Neovascularization 4
C11.204.299 Corneal Opacity 31
C11.204.431 Corneal Wavefront Aberration 6
C11.204.497 Iridocorneal Endothelial Syndrome 2
C11.204.564 Keratitis 126
C11.204.627 Keratoconus 93
C11.204.720 Limbal Stem Cell Deficiency
C11.204.813 Trachoma 64
C11.270 Eye Diseases, Hereditary 57
C11.270.019 Aicardi Syndrome
C11.270.040 Albinism 17
C11.270.060 Aniridia 18
C11.270.142 Choroideremia 3
C11.270.147 Coloboma 14
C11.270.151 Cone Dystrophy
C11.270.152 Cone-Rod Dystrophies
C11.270.162 Corneal Dystrophies, Hereditary 63
C11.270.162.218 Corneal Dystrophy, Juvenile Epithelial of Meesmann 1
C11.270.162.438 Fuchs' Endothelial Dystrophy 15
C11.270.235 Duane Retraction Syndrome 9
C11.270.238 Familial Exudative Vitreoretinopathies
C11.270.240 Graves Ophthalmopathy 57
C11.270.468 Gyrate Atrophy 1
C11.270.516 Leber Congenital Amaurosis 6
C11.270.564 Optic Atrophies, Hereditary 5
C11.270.588 Optic Nerve Hypoplasia 1
C11.270.612 Retinal Degeneration 75
C11.270.660 Retinal Dysplasia 4
C11.270.684 Retinitis Pigmentosa 55
C11.270.862 Retinoblastoma 159
C11.270.872 Stargardt Disease 6
C11.270.881 Walker-Warburg Syndrome 4
C11.270.921 Weill-Marchesani Syndrome 1
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 213
C16.320.290 Eye Diseases, Hereditary 57
C16.320.290.019 Aicardi Syndrome
C16.320.290.040 Albinism 17
C16.320.290.078 Aniridia 18
C16.320.290.142 Choroideremia 3
C16.320.290.152 Cone-Rod Dystrophies
C16.320.290.162 Corneal Dystrophies, Hereditary 63
C16.320.290.162.204 Corneal Dystrophy, Juvenile Epithelial of Meesmann 1
C16.320.290.162.410 Fuchs' Endothelial Dystrophy 15
C16.320.290.235 Duane Retraction Syndrome 9
C16.320.290.352 Familial Exudative Vitreoretinopathies
C16.320.290.410 Graves Ophthalmopathy 57
C16.320.290.468 Gyrate Atrophy 1
C16.320.290.564 Optic Atrophies, Hereditary 5
C16.320.290.612 Optic Nerve Hypoplasia 1
C16.320.290.660 Retinal Dysplasia 4
C16.320.290.684 Retinitis Pigmentosa 55
C16.320.290.724 Stargardt Disease 6
C16.320.290.763 Vitelliform Macular Dystrophy 5
C16.320.290.842 Weill-Marchesani Syndrome 1

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Chorioretinal atrophy, progressive bifocal Disease MeSH Browser

Congenital Corneal Opacities, Cornea Guttata, and Corectopia Disease MeSH Browser

Corneal Degeneration, Ribbonlike, with Deafness Disease MeSH Browser

Corneal Dystrophy, Band-Shaped Disease MeSH Browser

Corneal Dystrophy, Central Type Disease MeSH Browser

Corneal Dystrophy, Congenital Stromal Disease MeSH Browser

Corneal Dystrophy, Crystalline, of Schnyder Disease MeSH Browser

Corneal Dystrophy, Endothelial, X-Linked Disease MeSH Browser

Corneal Dystrophy, Fleck Disease MeSH Browser

Corneal Dystrophy, Lattice Type IIIA Disease MeSH Browser

Corneal Dystrophy, Lisch Epithelial Disease MeSH Browser

Corneal Dystrophy, Posterior Amorphous Disease MeSH Browser

Corneal Dystrophy, Posterior Polymorphous, 1 Disease MeSH Browser

Corneal Dystrophy, Posterior Polymorphous, 2 Disease MeSH Browser

Corneal Dystrophy, Posterior Polymorphous, 3 Disease MeSH Browser

Corneal Dystrophy, Subepithelial Mucinous Disease MeSH Browser

Corneal Endothelial Dystrophy 1 Disease MeSH Browser

Corneal cerebellar syndrome Disease MeSH Browser

Corneal dystrophy Avellino type Disease MeSH Browser

Corneal dystrophy and perceptive deafness Disease MeSH Browser

Corneal dystrophy of Bowman layer, type 1 Disease MeSH Browser

Corneal dystrophy, Thiel-Behnke type Disease MeSH Browser

Corneal dystrophy, gelatinous drop-like Disease MeSH Browser

Corneal endothelial dystrophy type 2 Disease MeSH Browser

Corneodermatoosseous syndrome Disease MeSH Browser

Dermochondrocorneal dystrophy of François Disease MeSH Browser

Endothelial Dystrophy, Congenital Hereditary, with Nail Hypoplasia Disease MeSH Browser

Epithelial Recurrent Erosion Dystrophy Disease MeSH Browser

Groenouw type I corneal dystrophy Disease MeSH Browser

Ichthyosiform erythroderma, corneal involvement, deafness Disease MeSH Browser

Judge Misch Wright syndrome Disease MeSH Browser

Kuster Majewski Hammerstein syndrome Disease MeSH Browser

Lattice Corneal Dystrophy, Type II Disease MeSH Browser

Lattice corneal dystrophy type 1 Disease MeSH Browser

Macular Corneal Dystrophy, Type II Disease MeSH Browser

Macular Dystrophy, Fenestrated Sheen Type Disease MeSH Browser

Macular Dystrophy, Retinal, 2 Disease MeSH Browser

Macular dystrophy, corneal type 1 Disease MeSH Browser

Macular dystrophy, retinal, 1, North Carolina type Disease MeSH Browser

Meretoja syndrome Disease MeSH Browser

Mousa Al din Al Nassar syndrome Disease MeSH Browser

O'Donnell Pappas syndrome Disease MeSH Browser

Oculodental syndrome Rutherfurd syndrome Disease MeSH Browser

Pseudoinflammatory fundus dystrophy, Finnish type Disease MeSH Browser

Sammartino De Crecchio Syndrome Disease MeSH Browser

Spondyloepiphyseal Dysplasia With Punctate Corneal Dystrophy Disease MeSH Browser

Sveinsson Chorioretinal Atrophy Disease MeSH Browser

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