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Retinal Dysplasia
Congenital, often bilateral, retinal abnormality characterized by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes 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
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therapy
urine
veterinary
virology
树号:
C11.250.666, C11.270.660, C11.768.660, C16.131.384.784, C16.320.290.660
MeSH 单一 ID:
D015792
进入的组:
Dysplasia, Retinal
Dysplasias, Retinal
Retinal Dysplasias
早前的内容:
Retina/abnormalities (1966-1989)
Retinal Degeneration (1970-1989)
All MeSH Categories
Diseases Category
Eye Diseases [C11]
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]
All MeSH Categories
Diseases Category
Eye Diseases [C11]
Eye Diseases, Hereditary [C11.270]
Aicardi Syndrome [C11.270.019]
Albinism [C11.270.040]
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Aniridia [C11.270.060]
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Choroideremia [C11.270.142]
Coloboma [C11.270.147]
add_circle
Cone Dystrophy [C11.270.151]
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Cone-Rod Dystrophies [C11.270.152]
Corneal Dystrophies, Hereditary [C11.270.162]
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Duane Retraction Syndrome [C11.270.235]
Familial Exudative Vitreoretinopathies [C11.270.238]
Graves Ophthalmopathy [C11.270.240]
Gyrate Atrophy [C11.270.468]
Leber Congenital Amaurosis [C11.270.516]
Optic Atrophies, Hereditary [C11.270.564]
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Optic Nerve Hypoplasia [C11.270.588]
Retinal Degeneration [C11.270.612]
Retinal Dysplasia [C11.270.660]
Retinitis Pigmentosa [C11.270.684]
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Retinoblastoma [C11.270.862]
Stargardt Disease [C11.270.872]
Walker-Warburg Syndrome [C11.270.881]
Weill-Marchesani Syndrome [C11.270.921]
All MeSH Categories
Diseases Category
Eye Diseases [C11]
Retinal Diseases [C11.768]
Angioid Streaks [C11.768.094]
Central Serous Chorioretinopathy [C11.768.175]
Cone Dystrophy [C11.768.216]
Diabetic Retinopathy [C11.768.257]
Epiretinal Membrane [C11.768.328]
Familial Exudative Vitreoretinopathies [C11.768.337]
Hypertensive Retinopathy [C11.768.346]
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Leber Congenital Amaurosis [C11.768.364]
Retinal Artery Occlusion [C11.768.400]
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Retinal Degeneration [C11.768.585]
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Retinal Detachment [C11.768.648]
Retinal Dysplasia [C11.768.660]
Retinal Hemorrhage [C11.768.710]
Retinal Neoplasms [C11.768.717]
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Retinal Neovascularization [C11.768.725]
Retinal Perforations [C11.768.740]
Retinal Telangiectasis [C11.768.748]
Retinal Vasculitis [C11.768.757]
Retinal Vein Occlusion [C11.768.760]
Retinitis [C11.768.773]
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Retinopathy of Prematurity [C11.768.836]
Vitreoretinopathy, Proliferative [C11.768.890]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Eye Abnormalities [C16.131.384]
Aniridia [C16.131.384.079]
add_circle
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]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Eye Diseases, Hereditary [C16.320.290]
Aicardi Syndrome [C16.320.290.019]
Albinism [C16.320.290.040]
add_circle
Aniridia [C16.320.290.078]
add_circle
Choroideremia [C16.320.290.142]
Cone-Rod Dystrophies [C16.320.290.152]
Corneal Dystrophies, Hereditary [C16.320.290.162]
add_circle
Duane Retraction Syndrome [C16.320.290.235]
Familial Exudative Vitreoretinopathies [C16.320.290.352]
Graves Ophthalmopathy [C16.320.290.410]
Gyrate Atrophy [C16.320.290.468]
Optic Atrophies, Hereditary [C16.320.290.564]
add_circle
Optic Nerve Hypoplasia [C16.320.290.612]
Retinal Dysplasia [C16.320.290.660]
Retinitis Pigmentosa [C16.320.290.684]
add_circle
Stargardt Disease [C16.320.290.724]
Vitelliform Macular Dystrophy [C16.320.290.763]
Weill-Marchesani Syndrome [C16.320.290.842]
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