Belgian Genetic Tests database
Wagner disease
| Name: |
Wagner disease
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| 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.
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| ORPHAcode: |
898
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| Synonyms: |
Dominant hyaloideoretinal dystrophy of Wagner
VCAN-related vitreoretinopathy
Vitreoretinal degeneration, Wagner type
Wagner syndrome
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| XREF(s): | |
| Analyte(s): | |
| Created: |
13 May 2019 - 01:02
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| Changed: |
22 Jun 2023 - 16:14
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