RetinoGenetics
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Alagille syndrome
Alstrom syndrome
Bardet-Biedl syndrome
Leber congenital amaurosis
Retinitis pigmentosa
Stargardt disease
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Quick Search:
RetinoGenetics ID:
Gene symbol:
Disease:
Top 5 genes
ABCA4:
855
USH2A:
395
RPGR:
367
WFS1:
205
CRB1:
132
Top 5 diseases
Stargardt disease:
661
Retinitis pigmentosa,X-linked:
417
Retinitis pigmentosa,AR:
367
Usher syndrome type II:
360
Leber congenital amaurosis:
331
Data summary
Publications :
991
Phenotypes :
178
Genes :
207
Mutations :
4583
SNVs :
3411
InDels :
1172
Last Update :
05/11/2017
Browse by chromosome
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