EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
2.3.1.135 | Retinitis Pigmentosa |
29973277 |
A novel LRAT mutation affecting splicing in a family with early onset retinitis pigmentosa. |
causal interaction ongoing research unassigned |
2 1 0 |
2.3.1.135 | Hypercholesterolemia |
25906639 |
Asteroid hyalosis--current state of knowledge. |
unassigned |
0 |
2.3.1.135 | Hypertension |
25906639 |
Asteroid hyalosis--current state of knowledge. |
unassigned |
0 |
2.3.1.135 | Leber Congenital Amaurosis |
25906639 |
Asteroid hyalosis--current state of knowledge. |
unassigned |
0 |
2.3.1.135 | Retinitis Pigmentosa |
25906639 |
Asteroid hyalosis--current state of knowledge. |
unassigned |
0 |
2.3.1.135 | Blindness |
22531707 |
Chemical chaperone TUDCA preserves cone photoreceptors in a mouse model of Leber congenital amaurosis. |
unassigned |
0 |
2.3.1.135 | Leber Congenital Amaurosis |
22531707 |
Chemical chaperone TUDCA preserves cone photoreceptors in a mouse model of Leber congenital amaurosis. |
unassigned |
0 |
2.3.1.135 | Blindness |
21555576 |
Cone opsin determines the time course of cone photoreceptor degeneration in Leber congenital amaurosis. |
causal interaction unassigned |
2 0 |
2.3.1.135 | Leber Congenital Amaurosis |
21555576 |
Cone opsin determines the time course of cone photoreceptor degeneration in Leber congenital amaurosis. |
causal interaction unassigned |
2 0 |
2.3.1.135 | Retinal Dystrophies |
21555576 |
Cone opsin determines the time course of cone photoreceptor degeneration in Leber congenital amaurosis. |
causal interaction unassigned |
2 0 |