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Aniridia
A congenital abnormality in which there is only a rudimentary iris. This is due to the failure of the optic cup to grow. Aniridia also occurs in a hereditary form, usually autosomal dominant.
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:
C11.250.060, C11.270.060, C11.941.375.060, C16.131.384.079, C16.320.290.078
MeSH 单一 ID:
D015783
进入的组:
Irideremia
Absent Iris
Congenital Aniridia
早前的内容:
Chromosome Deletion (1975-1989)
Iris/abnormalities (1966-1989)
All MeSH Categories
Diseases Category
Eye Diseases [C11]
Eye Abnormalities [C11.250]
Aniridia [C11.250.060]
WAGR Syndrome []
add_circle
Anophthalmos [C11.250.080]
Blepharophimosis [C11.250.090]
Choroidal Effusions [C11.250.105]
add_circle
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]
add_circle
Aniridia [C11.270.060]
WAGR Syndrome []
add_circle
Choroideremia [C11.270.142]
Coloboma [C11.270.147]
add_circle
Cone Dystrophy [C11.270.151]
add_circle
Cone-Rod Dystrophies [C11.270.152]
Corneal Dystrophies, Hereditary [C11.270.162]
add_circle
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]
add_circle
Optic Nerve Hypoplasia [C11.270.588]
Retinal Degeneration [C11.270.612]
Retinal Dysplasia [C11.270.660]
Retinitis Pigmentosa [C11.270.684]
add_circle
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]
Uveal Diseases [C11.941]
Iris Diseases [C11.941.375]
Aniridia [C11.941.375.060]
WAGR Syndrome []
add_circle
Exfoliation Syndrome [C11.941.375.285]
Iridocorneal Endothelial Syndrome [C11.941.375.322]
Iridocyclitis [C11.941.375.360]
Iris Neoplasms [C11.941.375.375]
Iritis [C11.941.375.385]
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]
WAGR Syndrome []
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]
WAGR Syndrome []
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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