Belgian Genetic Tests database
Stargardt disease
| Name: |
Stargardt disease
|
| Description: |
A rare ophthalmic disorder that is usually characterized by a progressive loss of central vision associated with irregular macular and perimacular yellow-white fundus flecks, and a so-called ''beaten bronze'' atrophic central macular lesion.
|
| ORPHAcode: |
827
|
| Synonyms: |
Fundus flavimaculatus
Stargardt 1
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| XREF(s): | |
| Analyte(s): | |
| Created: |
13 May 2019 - 01:02
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| Changed: |
22 Jun 2023 - 16:14
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