You are using an outdated browser. Please upgrade your browser to improve your experience.

Wagner disease

Disease Summary
Associated Targets (2)
Tbio

2


GARD Rare
Mondo Description Wagner disease is a rare hereditary vitreoretinopathy characterized by an anomaleous vitreous associated with myopia, cataract, chorioretinal atrophy, and peripheral tractional or rhegmatogenous retinal detachment.
Uniprot Description A rare vitreoretinopathy characterized by an optically empty vitreous cavity with fibrillary condensations and a preretinal avascular membrane. Other optical features include progressive chorioretinal atrophy, perivascular sheating, subcapsular cataract and myopia.
Mondo Term and Equivalent IDs
MONDO:0007740:  Wagner disease
GARD:0007871: 
MESH:C536075: 
Orphanet:898: 
SCTID:232064001: 
UMLS:C1840452: