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Eye Abnormalities
Congenital absence of or defects in structures of the eye; may also be hereditary.
推出的年份: 1990
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
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:
C11.250, C16.131.384
MeSH 单一 ID:
D005124
进入的组:
Abnormalities, Eye
Abnormality, Eye
Eye Abnormality
早前的内容:
Eye/abnormalities (1977-1989)
specific eye heading/abnormalities (1977-1989)
All MeSH Categories
Diseases Category
Eye Diseases [C11]
Asthenopia [C11.093]
Cogan Syndrome [C11.180]
Conjunctival Diseases [C11.187]
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Corneal Diseases [C11.204]
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Eye Abnormalities [C11.250]
Aniridia [C11.250.060]
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Anophthalmos [C11.250.080]
Blepharophimosis [C11.250.090]
Choroidal Effusions [C11.250.105]
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Coloboma [C11.250.110]
Ectopia Lentis [C11.250.300]
Familial Exudative Vitreoretinopathies [C11.250.345]
Fraser Syndrome [C11.250.390]
Hydrophthalmos [C11.250.480]
Microphthalmos [C11.250.566]
Persistent Hyperplastic Primary Vitreous [C11.250.616]
Retinal Dysplasia [C11.250.666]
Eye Diseases, Hereditary [C11.270]
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Eye Hemorrhage [C11.290]
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Eye Infections [C11.294]
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Eye Injuries [C11.297]
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Eye Manifestations [C11.300]
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Eye Neoplasms [C11.319]
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Eyelid Diseases [C11.338]
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Lacrimal Apparatus Diseases [C11.496]
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Lens Diseases [C11.510]
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Ocular Hypertension [C11.525]
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Ocular Hypotension [C11.540]
Ocular Motility Disorders [C11.590]
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Optic Nerve Diseases [C11.640]
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Orbital Diseases [C11.675]
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Pupil Disorders [C11.710]
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Refractive Errors [C11.744]
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Retinal Diseases [C11.768]
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Scleral Diseases [C11.790]
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Uveal Diseases [C11.941]
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Vision Disorders [C11.966]
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Vitreous Detachment [C11.980]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Drug-Induced [C16.131.042]
Abnormalities, Multiple [C16.131.077]
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Abnormalities, Radiation-Induced [C16.131.080]
Abnormalities, Severe Teratoid [C16.131.085]
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Aicardi Syndrome [C16.131.162]
Cardiovascular Abnormalities [C16.131.240]
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Chromosome Disorders [C16.131.260]
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Congenital Microtia [C16.131.287]
Digestive System Abnormalities [C16.131.314]
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Eye Abnormalities [C16.131.384]
Aniridia [C16.131.384.079]
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Anophthalmos [C16.131.384.159]
Blepharophimosis [C16.131.384.190]
Coloboma [C16.131.384.282]
Ectopia Lentis [C16.131.384.405]
Familial Exudative Vitreoretinopathies [C16.131.384.424]
Fraser Syndrome [C16.131.384.442]
Hydrophthalmos [C16.131.384.480]
Microphthalmos [C16.131.384.666]
Persistent Hyperplastic Primary Vitreous [C16.131.384.725]
Retinal Dysplasia [C16.131.384.784]
Hernias, Diaphragmatic, Congenital [C16.131.433]
Lymphatic Abnormalities [C16.131.482]
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Musculoskeletal Abnormalities [C16.131.621]
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Nervous System Malformations [C16.131.666]
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Respiratory System Abnormalities [C16.131.740]
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Situs Inversus [C16.131.810]
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Skin Abnormalities [C16.131.831]
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Stomatognathic System Abnormalities [C16.131.850]
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Thyroid Dysgenesis [C16.131.894]
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Urogenital Abnormalities [C16.131.939]
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