|
Severe myopia
|
0.030 |
GeneticVariation
|
disease |
BEFREE |
This study is managed to discover the connection between some single nucleotide polymorphism (located at MYP10 and MYP15) and Han Chinese HM.
|
31134845 |
2019 |
|
Myopia
|
0.030 |
GeneticVariation
|
disease |
BEFREE |
Associations were found at known myopia locus MYP10 on chromosome 8p23 and MYP15 on chromosome 10q21.1.
|
23049088 |
2012 |
|
Myopia
|
0.030 |
Biomarker
|
disease |
BEFREE |
Participants were divided into three groups: high myopia group (myopia of 6-10 diopters [D]), severe high myopia group (myopia ≥ 10 D), and control group (myopia ≤ 0.5 D).
|
22899762 |
2012 |
|
Severe myopia
|
0.030 |
GeneticVariation
|
disease |
BEFREE |
Participants were divided into three groups: high myopia group (myopia of 6-10 diopters [D]), severe high myopia group (myopia ≥ 10 D), and control group (myopia ≤ 0.5 D).
|
22899762 |
2012 |
|
Severe myopia
|
0.030 |
Biomarker
|
disease |
BEFREE |
We provide evidence for the association of MYP10 at 8p23 and MYP15 at 10p21.1 with high myopia in the French population and refine these regions of association.
|
23049088 |
2012 |
|
Myopia
|
0.030 |
GeneticVariation
|
disease |
BEFREE |
Probands with extreme myopia (-10 DS or worse) showed the highest study participation rate of 56%, when compared to high (-5 DS < -10 DS) (20%), moderate (-3 DS < - 5 DS) (18%) and low myopia (-0.5 DS < -3 DS) (10%).
|
16283990 |
2005 |
|
Congenital ocular coloboma (disorder)
|
0.010 |
Biomarker
|
disease |
BEFREE |
Of those patients, 67 (29%) had TRD (retinopathy of prematurity, persistent fetal vasculature, or familial exudative vitreoretinopathy), 51 (22%) had rhegmatogenous retinal detachment (myopia, X-linked retinoschisis, or Stickler syndrome), 60 (26%) had traumatic RD, and 53 (23%) were due to other types of RD, such as Coats disease or coloboma.
|
28858062 |
2018 |
|
Retinal Detachment
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Of those patients, 67 (29%) had TRD (retinopathy of prematurity, persistent fetal vasculature, or familial exudative vitreoretinopathy), 51 (22%) had rhegmatogenous retinal detachment (myopia, X-linked retinoschisis, or Stickler syndrome), 60 (26%) had traumatic RD, and 53 (23%) were due to other types of RD, such as Coats disease or coloboma.
|
28858062 |
2018 |
|
Exudative retinopathy
|
0.010 |
Biomarker
|
disease |
BEFREE |
Of those patients, 67 (29%) had TRD (retinopathy of prematurity, persistent fetal vasculature, or familial exudative vitreoretinopathy), 51 (22%) had rhegmatogenous retinal detachment (myopia, X-linked retinoschisis, or Stickler syndrome), 60 (26%) had traumatic RD, and 53 (23%) were due to other types of RD, such as Coats disease or coloboma.
|
28858062 |
2018 |
|
Stickler syndrome (disorder)
|
0.010 |
Biomarker
|
disease |
BEFREE |
Of those patients, 67 (29%) had TRD (retinopathy of prematurity, persistent fetal vasculature, or familial exudative vitreoretinopathy), 51 (22%) had rhegmatogenous retinal detachment (myopia, X-linked retinoschisis, or Stickler syndrome), 60 (26%) had traumatic RD, and 53 (23%) were due to other types of RD, such as Coats disease or coloboma.
|
28858062 |
2018 |
|
Rhegmatogenous retinal detachment
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Of those patients, 67 (29%) had TRD (retinopathy of prematurity, persistent fetal vasculature, or familial exudative vitreoretinopathy), 51 (22%) had rhegmatogenous retinal detachment (myopia, X-linked retinoschisis, or Stickler syndrome), 60 (26%) had traumatic RD, and 53 (23%) were due to other types of RD, such as Coats disease or coloboma.
|
28858062 |
2018 |
|
Stickler syndrome, type 1
|
0.010 |
Biomarker
|
disease |
BEFREE |
Of those patients, 67 (29%) had TRD (retinopathy of prematurity, persistent fetal vasculature, or familial exudative vitreoretinopathy), 51 (22%) had rhegmatogenous retinal detachment (myopia, X-linked retinoschisis, or Stickler syndrome), 60 (26%) had traumatic RD, and 53 (23%) were due to other types of RD, such as Coats disease or coloboma.
|
28858062 |
2018 |