Eye Diseases, Hereditary [dědičné nemoci očí]

topical
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Terms

oči - nemoci dědičné
vrozené nemoci oka

 

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

C Diseases
C11 Eye Diseases 1 495
C11.093 Asthenopia 20
C11.204 Corneal Diseases 254
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
C11.270.468 Gyrate Atrophy 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
C11.290 Eye Hemorrhage 23
C11.294 Eye Infections 74
C11.297 Eye Injuries 372
C11.319 Eye Neoplasms 291
C11.338 Eyelid Diseases 144
C11.510 Lens Diseases 42
C11.675 Orbital Diseases 152
C11.768 Retinal Diseases 404
C11.941 Uveal Diseases 47
C11.966 Vision Disorders 710
C16.320.051 Alagille Syndrome 19
C16.320.100 Brugada Syndrome 40
C16.320.129 CADASIL 8
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
C16.320.290.019 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
C16.320.290.235 Duane Retraction Syndrome 9
C16.320.290.410 Graves Ophthalmopathy 58
C16.320.290.468 Gyrate Atrophy 1
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
C16.320.290.842 Weill-Marchesani Syndrome 1
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 2
C16.320.365 Hemoglobinopathies 68
C16.320.467 Kallmann Syndrome 10
C16.320.480 Kartagener Syndrome 46
C16.320.488 Laminopathies 2
C16.320.540 Marfan Syndrome 105
C16.320.577 Muscular Dystrophies 141
C16.320.728 Osteochondrodysplasias 125
C16.320.784 Pelger-Huet Anomaly 7
C16.320.812 Pycnodysostosis 2
C16.320.925 Werner Syndrome 14

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