encyclopedia of medical concepts
ψ 
ψ 

Eye Diseases, Hereditary

More information in Books or onNLM PubMed
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.     
Examples Aicardi Syndrome; Albinism; Aniridia; Choroideremia; Corneal Dystrophies, Hereditary; Duane Retraction Syndrome; Gyrate Atrophy; Leber Congenital Amaurosis; Optic Atrophies, Hereditary; Retinal Dysplasia; Retinitis Pigmentosa; Graves Ophthalmopathy; Walker-Warburg Syndrome; Weill-Marchesani Syndrome
Other names Hereditary Eye Disease; Eye Disease, Hereditary; Diseases, Hereditary Eye; Disease, Hereditary Eye; Hereditary Eye Diseases
 
SubstanceCAS Registry & nameCategoriesSource
Vitreoretinochoroidopathy dominant  0   *Retinal Degeneration *Eye Diseases, Hereditary *Choroid Diseases.

To share this definition, click "text" (Facebook, Twitter) or "link" (blog, mail) then paste text link
Ads by Google

Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

Warning: the drugs or drug combinations referred to here may be similar or related, but are not be the same ones and may not have the same pharmacological action as other substances described on the same page or in the same row. Please refer to product monograph or to your doctor
This website is accredited by Health On the Net Foundation. Click to verify.
We comply with the HONcode standard for trustworthy health information: verify here.
About Reference.MD Privacy