Concept information
Preferred term
Eye Diseases, Hereditary
Type
-
Topical Descriptor
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
- Eye Disease, Hereditary
- Hereditary Eye Disease
- Hereditary Eye Diseases
Scope note
- 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.
History note
- 90
In other languages
-
Finnish
-
hereditaariset silmäsairaudet
-
hereditaariset silmätaudit
-
hereditääriset silmäsairaudet
-
hereditääriset silmätaudit
-
perinnölliset silmäsairaudet
-
periytyvät silmäsairaudet
-
periytyvät silmätaudit
-
Swedish
URI
http://www.yso.fi/onto/mesh/D015785
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