Home Contact Sitemap

eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease open-angle glaucoma
Comorbidity C0456909|blindness
Sentences 8
PubMedID- 23258653 Risk factors for blindness in patients with open-angle glaucoma followed-up for at least 15 years.
PubMedID- 21051332 Mutations in wd repeat domain 36 gene (wdr36) play a causative role in some forms of primary open-angle glaucoma, a leading cause of blindness worldwide.
PubMedID- 24082707 blindness due to primary open-angle glaucoma is more difficult to prevent and medication in open angle glaucoma could prevent the progression of the disease (grade a).
PubMedID- 24647762 Mutations in the human homolog of utp21, wdr36, have been associated with adult-onset primary open-angle glaucoma, a leading cause of blindness worldwide.
PubMedID- 21887073 Primary open-angle glaucoma was the cause of blindness in 25 (5%) subjects, most of whom were unemployed and had little education.
PubMedID- 24466140 Mutations in wdr36, the human utp21 gene, have been associated with primary open angle glaucoma, a leading cause of blindness [14].
PubMedID- 23932216 Purpose: to determine the lifetime risk and duration of blindness in patients with manifest open-angle glaucoma (oag).
PubMedID- 24823760 Objective: to determine the longitudinal trends in the probability of blindness due to open-angle glaucoma (oag) in olmsted county, minnesota, from 1965 to 2009.

Page: 1