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Optic Nerve Hypoplasia
A group of rare genetic disorders characterized by underdeveloped OPTIC NERVES, resulting in increased incidences of vision impairment, CONGENITAL NYSTAGMUS and STRABISMUS. It may be syndromic, and is often associated with CNS malformations.
推出的年份: 2020
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:
C10.292.700.463, C10.500.760, C11.270.588, C11.640.522, C16.131.666.763, C16.320.290.612
MeSH 单一 ID:
D000080344
进入的组:
Hypoplasia, Optic Nerve
Superior Segmental Optic Nerve Hypoplasia
Superior Segmental Optic Hypoplasia
早前的内容:
Optic Nerve/abnormalities (1969-2019)
All MeSH Categories
Diseases Category
Nervous System Diseases [C10]
Cranial Nerve Diseases [C10.292]
Optic Nerve Diseases [C10.292.700]
Optic Atrophy [C10.292.700.225]
add_circle
Optic Disk Drusen [C10.292.700.450]
Optic Nerve Hypoplasia [C10.292.700.463]
Optic Nerve Injuries [C10.292.700.475]
add_circle
Optic Nerve Neoplasms [C10.292.700.500]
add_circle
Optic Neuritis [C10.292.700.550]
add_circle
Optic Neuropathy, Ischemic [C10.292.700.600]
Papilledema [C10.292.700.900]
All MeSH Categories
Diseases Category
Nervous System Diseases [C10]
Nervous System Malformations [C10.500]
Agenesis of Corpus Callosum [C10.500.034]
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Central Nervous System Cysts [C10.500.142]
add_circle
Central Nervous System Vascular Malformations [C10.500.190]
add_circle
Dandy-Walker Syndrome [C10.500.205]
Hereditary Sensory and Autonomic Neuropathies [C10.500.250]
add_circle
Hereditary Sensory and Motor Neuropathy [C10.500.300]
add_circle
Hydranencephaly [C10.500.450]
Malformations of Cortical Development [C10.500.507]
add_circle
Neural Tube Defects [C10.500.680]
add_circle
Optic Nerve Hypoplasia [C10.500.760]
Septo-Optic Dysplasia [C10.500.760.500]
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]
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]
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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]
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]
Optic Nerve Diseases [C11.640]
Low Tension Glaucoma [C11.640.225]
Optic Atrophy [C11.640.451]
add_circle
Optic Disk Drusen [C11.640.513]
Optic Nerve Hypoplasia [C11.640.522]
Optic Nerve Injuries [C11.640.530]
add_circle
Optic Nerve Neoplasms [C11.640.544]
add_circle
Optic Neuritis [C11.640.576]
add_circle
Optic Neuropathy, Ischemic [C11.640.643]
Papilledema [C11.640.710]
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Nervous System Malformations [C16.131.666]
Agenesis of Corpus Callosum [C16.131.666.034]
add_circle
Central Nervous System Cysts [C16.131.666.142]
add_circle
Central Nervous System Vascular Malformations [C16.131.666.190]
add_circle
Dandy-Walker Syndrome [C16.131.666.205]
Hereditary Sensory and Autonomic Neuropathies [C16.131.666.310]
add_circle
Hereditary Sensory and Motor Neuropathy [C16.131.666.300]
add_circle
Hydranencephaly [C16.131.666.450]
Malformations of Cortical Development [C16.131.666.507]
add_circle
Neural Tube Defects [C16.131.666.680]
add_circle
Optic Nerve Hypoplasia [C16.131.666.763]
Septo-Optic Dysplasia [C16.131.666.763.500]
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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