Optic Nerve Hypoplasia [hypoplazie optického nervu]

topical
1
Terms

hypoplasie optického nervu
hypoplazie horního segmentu zrakového nervu
hypoplázie horního segmentu zrakového nervu
hypoplázie optického nervu

 

Superior Segmental Optic Hypoplasia
Superior Segmental Optic Nerve Hypoplasia

Persistent link   https://www.medvik.cz/link/D000080344
Definition

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.

DUI
D000080344 MeSH Browser
CUI
M000647104
Previous indexing
Optic Nerve/abnormalities (1969-2019)
History note
2020
Public note
2020

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
DI
diagnosis 1
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology
GE
genetics
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy
UR
urine
VE
veterinary
VI
virology

C Diseases
C10 Nervous System Diseases 1 879
C10.292 Cranial Nerve Diseases 60
C10.292.700 Optic Nerve Diseases 118
C10.292.700.225 Optic Atrophy 51
C10.292.700.450 Optic Disk Drusen 18
C10.292.700.463 Optic Nerve Hypoplasia 1
C10.292.700.475 Optic Nerve Injuries 12
C10.292.700.500 Optic Nerve Neoplasms 6
C10.292.700.550 Optic Neuritis 130
C10.292.700.600 Optic Neuropathy, Ischemic 32
C10.292.700.900 Papilledema 57
C10.500 Nervous System Malformations 80
C10.500.034 Agenesis of Corpus Callosum 12
C10.500.142 Central Nervous System Cysts 27
C10.500.190 Central Nervous System Vascular Malformations 20
C10.500.198 Congenital Cranial Dysinnervation Disorders
C10.500.205 Dandy-Walker Syndrome 6
C10.500.250 Hereditary Sensory and Autonomic Neuropathies 26
C10.500.300 Hereditary Sensory and Motor Neuropathy 71
C10.500.450 Hydranencephaly 3
C10.500.507 Malformations of Cortical Development 50
C10.500.680 Neural Tube Defects 77
C10.500.760 Optic Nerve Hypoplasia 1
C10.500.760.500 Septo-Optic Dysplasia 15
C11 Eye Diseases 1 491
C11.270 Eye Diseases, Hereditary 57
C11.270.019 Aicardi Syndrome
C11.270.040 Albinism 17
C11.270.060 Aniridia 18
C11.270.142 Choroideremia 3
C11.270.147 Coloboma 14
C11.270.151 Cone Dystrophy
C11.270.152 Cone-Rod Dystrophies
C11.270.162 Corneal Dystrophies, Hereditary 63
C11.270.235 Duane Retraction Syndrome 9
C11.270.238 Familial Exudative Vitreoretinopathies
C11.270.240 Graves Ophthalmopathy 58
C11.270.468 Gyrate Atrophy 1
C11.270.516 Leber Congenital Amaurosis 6
C11.270.564 Optic Atrophies, Hereditary 5
C11.270.588 Optic Nerve Hypoplasia 1
C11.270.612 Retinal Degeneration 75
C11.270.660 Retinal Dysplasia 4
C11.270.684 Retinitis Pigmentosa 56
C11.270.862 Retinoblastoma 159
C11.270.872 Stargardt Disease 6
C11.270.881 Walker-Warburg Syndrome 4
C11.270.921 Weill-Marchesani Syndrome 1
C11.640 Optic Nerve Diseases 118
C11.640.225 Low Tension Glaucoma 15
C11.640.451 Optic Atrophy 51
C11.640.513 Optic Disk Drusen 18
C11.640.522 Optic Nerve Hypoplasia 1
C11.640.530 Optic Nerve Injuries 12
C11.640.544 Optic Nerve Neoplasms 6
C11.640.576 Optic Neuritis 130
C11.640.643 Optic Neuropathy, Ischemic 32
C11.640.710 Papilledema 57
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 749
C16.131.666 Nervous System Malformations 80
C16.131.666.034 Agenesis of Corpus Callosum 12
C16.131.666.142 Central Nervous System Cysts 27
C16.131.666.190 Central Nervous System Vascular Malformations 20
C16.131.666.198 Congenital Cranial Dysinnervation Disorders
C16.131.666.205 Dandy-Walker Syndrome 6
C16.131.666.300 Hereditary Sensory and Motor Neuropathy 71
C16.131.666.310 Hereditary Sensory and Autonomic Neuropathies 26
C16.131.666.450 Hydranencephaly 3
C16.131.666.507 Malformations of Cortical Development 50
C16.131.666.680 Neural Tube Defects 77
C16.131.666.763 Optic Nerve Hypoplasia 1
C16.131.666.763.500 Septo-Optic Dysplasia 15
C16.320 Genetic Diseases, Inborn 1 214
C16.320.290 Eye Diseases, Hereditary 57
C16.320.290.019 Aicardi Syndrome
C16.320.290.040 Albinism 17
C16.320.290.078 Aniridia 18
C16.320.290.142 Choroideremia 3
C16.320.290.152 Cone-Rod Dystrophies
C16.320.290.162 Corneal Dystrophies, Hereditary 63
C16.320.290.235 Duane Retraction Syndrome 9
C16.320.290.352 Familial Exudative Vitreoretinopathies
C16.320.290.410 Graves Ophthalmopathy 58
C16.320.290.468 Gyrate Atrophy 1
C16.320.290.564 Optic Atrophies, Hereditary 5
C16.320.290.612 Optic Nerve Hypoplasia 1
C16.320.290.660 Retinal Dysplasia 4
C16.320.290.684 Retinitis Pigmentosa 56
C16.320.290.724 Stargardt Disease 6
C16.320.290.763 Vitelliform Macular Dystrophy 5
C16.320.290.842 Weill-Marchesani Syndrome 1

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