Phenotype #0000315271

Individual ID 00424063
Associated disease WGVRP
Phenotype details ophtalmological examinations right, left eye: best corrected visual acuity: 20/20, 20/25; recent refraction spherical equivalent: -2, -0.25; past (presurgical) refraction spherical equivalent: not available, not available; axial length, mm: 24.69, 24.46; lens status: posterior chamber intraocular lens, posterior chamber intraocular lens; retinal detachment age, y:not available; surgery: cataract extraction/intraocular lens, cataract extraction/intraocular lens; optically empty vitreous: yes, yes; vitreal avascular membranes: yes, yes; retinal traction: moderate, moderate; chorioretinal atrophy: moderate, moderate; retinal pigmentary changes: moderate, moderate; ocular alignment: exotropia, exotropia; visual field: ring scotoma, ring scotoma
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite vitreoretinopathy, Wagner (WGVRP, Wagner syndrome)
Age/Examination 37y (37 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2022-11-16 15:54:07 +01:00 (CET)
Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.