Concept information
Preferred term
Eye Diseases, Hereditary
Type
-
mesh:Descriptor
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.
Broader concept
Narrower concepts
- Aicardi Syndrome
- Albinism
- Aniridia
- Choroideremia
- Coloboma
- Cone Dystrophy
- 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
- Retinoblastoma
- Walker-Warburg Syndrome
- Weill-Marchesani Syndrome
Entry terms
- Hereditary Eye Diseases
Allowable Qualifier(s)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemically induced (Qualifier)
- classification (Qualifier)
- complications (Qualifier)
- diagnosis (Qualifier)
- diagnostic imaging (Qualifier)
- diet therapy (Qualifier)
- drug therapy (Qualifier)
- economics (Qualifier)
- embryology (Qualifier)
- enzymology (Qualifier)
- epidemiology (Qualifier)
- ethnology (Qualifier)
- etiology (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- mortality (Qualifier)
- nursing (Qualifier)
- parasitology (Qualifier)
- pathology (Qualifier)
- physiopathology (Qualifier)
- prevention & control (Qualifier)
- psychology (Qualifier)
- radiotherapy (Qualifier)
- rehabilitation (Qualifier)
- surgery (Qualifier)
- therapy (Qualifier)
- urine (Qualifier)
- veterinary (Qualifier)
- virology (Qualifier)
In other languages
-
French
-
Maladie héréditaire de l'oeil
-
Maladies héréditaires des yeux
-
Maladies oculaires héréditaires
URI
http://data.loterre.fr/ark:/67375/JVR-R0FNLV2B-2
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