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Fuchs' Endothelial Dystrophy
Disorder caused by loss of endothelium of the central cornea. It is characterized by hyaline endothelial outgrowths on Descemet's membrane, epithelial blisters, reduced vision, and pain.
推出的年份: 1991(1975)
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
congenital
diagnosis
diagnostic imaging
diet therapy
drug therapy
economics
embryology
enzymology
epidemiology
ethnology
etiology
genetics
history
immunology
metabolism
microbiology
mortality
nursing
parasitology
pathology
physiopathology
prevention and control
psychology
radiotherapy
rehabilitation
surgery
therapy
urine
veterinary
virology
树号:
C11.204.236.438, C11.270.162.438, C16.320.290.162.410
MeSH 单一 ID:
D005642
进入的组:
Dystrophy, Fuchs' Endothelial
Endothelial Dystrophy, Fuchs'
Fuchs Atrophy
Fuchs Corneal Dystrophy
Fuchs Endothelial Corneal Dystrophy
Fuchs Endothelial Dystrophy
Fuch's Endothelial Dystrophy
Dystrophy, Fuch's Endothelial
Endothelial Dystrophy, Fuch's
Fuch Endothelial Dystrophy
Fuchs Dystrophy
All MeSH Categories
Diseases Category
Eye Diseases [C11]
Corneal Diseases [C11.204]
Corneal Dystrophies, Hereditary [C11.204.236]
Corneal Dystrophy, Juvenile Epithelial of Meesmann [C11.204.236.218]
Fuchs' Endothelial Dystrophy [C11.204.236.438]
All MeSH Categories
Diseases Category
Eye Diseases [C11]
Eye Diseases, Hereditary [C11.270]
Corneal Dystrophies, Hereditary [C11.270.162]
Corneal Dystrophy, Juvenile Epithelial of Meesmann [C11.270.162.218]
Fuchs' Endothelial Dystrophy [C11.270.162.438]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Eye Diseases, Hereditary [C16.320.290]
Corneal Dystrophies, Hereditary [C16.320.290.162]
Corneal Dystrophy, Juvenile Epithelial of Meesmann [C16.320.290.162.204]
Fuchs' Endothelial Dystrophy [C16.320.290.162.410]
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