Eye Diseases, Hereditary [dědičné nemoci očí]
- Terms
-
oči - nemoci dědičné
vrozené nemoci oka
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Hereditary Eye Diseases
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
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
Narrower terms
- Aicardi Syndrome
- Albinism
- Aniridia
- Choroideremia
- Coloboma
- Cone Dystrophy
- Cone-Rod Dystrophies
- Corneal Dystrophies, Hereditary
- Duane Retraction Syndrome
- Familial Exudative Vitreoretinopathies
- Graves Ophthalmopathy
- Gyrate Atrophy
- Leber Congenital Amaurosis
- Optic Atrophies, Hereditary
- Optic Nerve Hypoplasia
- Retinal Degeneration
- Retinal Dysplasia
- Retinitis Pigmentosa
- Retinoblastoma
- Stargardt Disease
- Vitelliform Macular Dystrophy
- Walker-Warburg Syndrome
- Weill-Marchesani Syndrome