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Retinitis Pigmentosa
Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition of pigment in the retina.
推出的年份:
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
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urine
veterinary
virology
树号:
C11.270.684, C11.768.585.658.500, C16.320.290.684
MeSH 单一 ID:
D012174
进入的组:
Tapetoretinal Degeneration
Tapetoretinal Degenerations
Pigmentary Retinopathy
Pigmentary Retinopathies
Retinopathies, Pigmentary
Retinopathy, Pigmentary
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]
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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]
Alstrom Syndrome [C11.270.684.249]
Bardet-Biedl Syndrome [C11.270.684.624]
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]
Retinal Degeneration [C11.768.585]
Retinal Dystrophies [C11.768.585.658]
Cone-Rod Dystrophies [C11.768.585.658.250]
Retinitis Pigmentosa [C11.768.585.658.500]
Kearns-Sayre Syndrome [C11.768.585.658.500.627]
Usher Syndromes [C11.768.585.658.500.813]
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]
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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]
Alstrom Syndrome [C16.320.290.684.249]
Usher Syndromes [C16.320.290.684.500]
Stargardt Disease [C16.320.290.724]
Vitelliform Macular Dystrophy [C16.320.290.763]
Weill-Marchesani Syndrome [C16.320.290.842]
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