Eye Diseases, Hereditary [dědičné nemoci očí]

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Terms

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Hereditary Eye Diseases

Persistent link   https://www.medvik.cz/link/D015785
Definition

Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder.

DUI
D015785 MeSH Browser
CUI
M0024182
Previous indexing
Eye Diseases/genetics (1966-1989)
History note
90
Public note
90

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 10
CO
complications 3
DI
diagnosis 19
DG
diagnostic imaging 3
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology 1
EH
ethnology
ET
etiology 11
GE
genetics 23
HI
history
IM
immunology
ME
metabolism 1
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 7
PP
physiopathology
PC
prevention & control 1
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery 4
TH
therapy 12
UR
urine
VE
veterinary
VI
virology

C Diseases
C11 Eye Diseases 1 495
C11.093 Asthenopia 20
C11.180 Cogan Syndrome 6
C11.187 Conjunctival Diseases 46
C11.204 Corneal Diseases 254
C11.250 Eye Abnormalities 107
C11.270 Eye Diseases, Hereditary 58
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
C11.290 Eye Hemorrhage 23
C11.294 Eye Infections 74
C11.297 Eye Injuries 372
C11.300 Eye Manifestations 293
C11.319 Eye Neoplasms 291
C11.338 Eyelid Diseases 144
C11.496 Lacrimal Apparatus Diseases 101
C11.510 Lens Diseases 42
C11.525 Ocular Hypertension 84
C11.540 Ocular Hypotension 4
C11.590 Ocular Motility Disorders 101
C11.640 Optic Nerve Diseases 118
C11.675 Orbital Diseases 152
C11.710 Pupil Disorders 25
C11.744 Refractive Errors 330
C11.768 Retinal Diseases 404
C11.790 Scleral Diseases 16
C11.941 Uveal Diseases 47
C11.966 Vision Disorders 710
C11.980 Vitreous Detachment 21
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 215
C16.320.033 Adrenal Hyperplasia, Congenital 226
C16.320.051 Alagille Syndrome 19
C16.320.060 alpha 1-Antitrypsin Deficiency 86
C16.320.070 Anemia, Hemolytic, Congenital 48
C16.320.077 Anemia, Hypoplastic, Congenital 3
C16.320.080 Ataxia Telangiectasia 48
C16.320.089 Autoimmune Lymphoproliferative Syndrome 2
C16.320.099 Blood Coagulation Disorders, Inherited 64
C16.320.100 Brugada Syndrome 40
C16.320.129 CADASIL 8
C16.320.144 Camurati-Engelmann Syndrome 6
C16.320.160 Cardiomyopathy, Hypertrophic, Familial 33
C16.320.165 CHARGE Syndrome 1
C16.320.170 Cherubism 1
C16.320.180 Chromosome Disorders 260
C16.320.184 Ciliopathies 9
C16.320.188 Costello Syndrome 3
C16.320.190 Cystic Fibrosis 1 330
C16.320.215 Donohue Syndrome 1
C16.320.240 Dwarfism 99
C16.320.290 Eye Diseases, Hereditary 58
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
C16.320.298 Familial Multiple Lipomatosis
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 2
C16.320.322 Genetic Diseases, X-Linked 60
C16.320.338 Genetic Diseases, Y-Linked 1
C16.320.355 Hajdu-Cheney Syndrome 6
C16.320.365 Hemoglobinopathies 68
C16.320.382 Hereditary Autoinflammatory Diseases 47
C16.320.400 Heredodegenerative Disorders, Nervous System 46
C16.320.413 Hyper-IgM Immunodeficiency Syndrome 4
C16.320.427 Hyperthyroxinemia, Familial Dysalbuminemic 2
C16.320.447 Imprinting Disorders
C16.320.467 Kallmann Syndrome 10
C16.320.480 Kartagener Syndrome 46
C16.320.488 Laminopathies 2
C16.320.495 Lennox Gastaut Syndrome 6
C16.320.510 Loeys-Dietz Syndrome 7
C16.320.540 Marfan Syndrome 105
C16.320.565 Metabolism, Inborn Errors 714
C16.320.577 Muscular Dystrophies 141
C16.320.590 Myasthenic Syndromes, Congenital 21
C16.320.600 Nail-Patella Syndrome 8
C16.320.700 Neoplastic Syndromes, Hereditary 144
C16.320.709 Oculocerebrorenal Syndrome 9
C16.320.714 Orofaciodigital Syndromes 7
C16.320.718 Osteoarthropathy, Primary Hypertrophic 127
C16.320.728 Osteochondrodysplasias 125
C16.320.737 Osteogenesis Imperfecta 106
C16.320.775 Pain Insensitivity, Congenital 10
C16.320.784 Pelger-Huet Anomaly 7
C16.320.798 Primary Immunodeficiency Diseases 48
C16.320.812 Pycnodysostosis 2
C16.320.831 Renal Tubular Transport, Inborn Errors 36
C16.320.850 Skin Diseases, Genetic 89
C16.320.925 Werner Syndrome 14
C16.320.962 Yellow Nail Syndrome

Achromatopsia 4 Disease MeSH Browser

Achromatopsia 5 Disease MeSH Browser

Acrootoocular Syndrome Disease MeSH Browser

Alacrima Disease MeSH Browser

Alacrima, Congenital Disease MeSH Browser

Ataxia-Microcephaly-Cataract Syndrome Disease MeSH Browser

Axenfeld-Rieger syndrome Disease MeSH Browser

Basal Laminar Drusen Disease MeSH Browser

Bestrophinopathy Disease MeSH Browser

Bothnia Retinal Dystrophy Disease MeSH Browser

CSNB1C Disease MeSH Browser

Cataract, Congenital Nuclear, Autosomal Recessive 1 Disease MeSH Browser

Cataract, Congenital Nuclear, Autosomal Recessive 2 Disease MeSH Browser

Cataract, Congenital Nuclear, Autosomal Recessive 3 Disease MeSH Browser

Cataract, Floriform Disease MeSH Browser

Cataract, Pulverulent Disease MeSH Browser

Cavitary Optic Disc Anomalies Disease MeSH Browser

Cholestasis with Gallstone, Ataxia, and Visual Disturbance Disease MeSH Browser

Cornea Plana 1 Disease MeSH Browser

Cornea Plana 2 Disease MeSH Browser

Enhanced S-Cone Syndrome Disease MeSH Browser

Fibrosis Of Extraocular Muscles, Congenital, 2 Disease MeSH Browser

Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement Disease MeSH Browser

Fibrosis of Extraocular Muscles, Congenital, 3B Disease MeSH Browser

Fibrosis of Extraocular Muscles, Congenital, 3C Disease MeSH Browser

Fleck Retina, Familial Benign Disease MeSH Browser

Foveal Hypoplasia with Anterior Segment Anomalies Disease MeSH Browser

Foveal Hypoplasia, Isolated Disease MeSH Browser

Glaucoma 1, Open Angle, P Disease MeSH Browser

Grouped Pigmentation of the Macula Disease MeSH Browser

Histiocytic Dermatoarthritis Disease MeSH Browser

Hyperopia, High Disease MeSH Browser

Hypomagnesemia 5, Renal, with Ocular Involvement Disease MeSH Browser

Iris Pigment Epithelium Anomalies Disease MeSH Browser

Joubert Syndrome 8 Disease MeSH Browser

Macular Dystrophy, X-Linked Disease MeSH Browser

Megalocornea Disease MeSH Browser

Microcephaly with Chorioretinopathy, Autosomal Recessive Disease MeSH Browser

Mydriasis, Congenital Disease MeSH Browser

Night Blindness, Congenital Stationary, Autosomal Dominant 1 Disease MeSH Browser

Night Blindness, Congenital Stationary, Autosomal Dominant 2 Disease MeSH Browser

Night Blindness, Congenital Stationary, Autosomal Dominant 3 Disease MeSH Browser

Night blindness, congenital stationary Disease MeSH Browser

Oguchi disease Disease MeSH Browser

Omphalocele, Diaphragmatic Hernia, And Radial Ray Defects Disease MeSH Browser

Ophthalmomandibulomelic Dysplasia Disease MeSH Browser

Peripapillary Atrophy, Beta Type Disease MeSH Browser

Persistent Hyperplastic Primary Vitreous, Autosomal Recessive Disease MeSH Browser

Pigmented Paravenous Chorioretinal Atrophy Disease MeSH Browser

Prolonged Electroretinal Response Suppression Disease MeSH Browser

Pseudopapilledema Disease MeSH Browser

Retinal Aplasia Disease MeSH Browser

Retinal Dystrophy, Early Onset Severe Disease MeSH Browser

Retinohepatoendocrinologic Syndrome Disease MeSH Browser

Rhegmatogenous Retinal Detachment, Autosomal Dominant Disease MeSH Browser

Spondyloocular Syndrome, Autosomal Recessive Disease MeSH Browser

Stickler Syndrome, Type I, Nonsyndromic Ocular Disease MeSH Browser

Vascular Hyalinosis Disease MeSH Browser

Vitreoretinochoroidopathy Disease MeSH Browser

Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia Disease MeSH Browser

Weill-Marchesani-Like Syndrome Disease MeSH Browser

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