Stargardt's disease
(UMLS:C0271093)
- Definition:
- A juvenile-onset macular dystrophy characterized by progressive loss of VISUAL ACUITY with normal acuity in peripheral VISUAL FIELDS. Other associated clinical features may include LIPOFUSCIN fundus autofluorescence, atrophy of the RETINAL PIGMENT EPITHELIUM, loss of color vision, PHOTOPHOBIA and PARACENTRAL SCOTOMA. Germline mutations in the ABCA4 gene have been identified in recessive and dominant diseases.
- UMLS ID:
- C0271093
- MeSH ID:
- N/A
Synonym(s)
1.
Stargardt's disease
2.
FFM - Fundus flavimaculatus
3.
Familial juvenile macular degeneration syndrome
4.
Fundus flavimaculatus
5.
STARGARDT SYNDROME
6.
Stargardt
7.
Stargardt Disease
8.
Stargardt disease
9.
fundus flavimaculatus
10.
stargardt's disease
Associated Drug(s)
| Name | Number of Reports | Reference(s) | Data Source | |
|---|---|---|---|---|
| 1 | Isotretinoin | FAERS: 8 | US FAERS | |
| 2 | Norgestrel | FAERS: 3 | OFFSIDES US FAERS | |
| 3 | histrelin | SIDER |
Powered by :
Page last updated at 2020-05-25 10:01:57 (Asia/Shanghai) | You are visitor No. 120241
Copyright © 2019-2020 Laboratory of Molecular Modeling and Design, Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology. All rights reserved.