Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormal full-field electroretinogram
Frequent (30-79%)HP:0030466
Chorioretinal atrophy
Frequent (30-79%)HP:0000533
Decreased visual acuity
Frequent (30-79%)HP:0007663
Near sighted
Frequent (30-79%)HP:0000545
Night blindness
Frequent (30-79%)HP:0000662
Pigmentary retinopathy
Frequent (30-79%)HP:0000580
Presenile cataracts
Frequent (30-79%)HP:0007819
Retinal detachment
Frequent (30-79%)HP:0000541
Ectopic fovea
Occasional (5-29%)HP:0025007
Exudative vitreoretinopathy
Occasional (5-29%)HP:0030490
Glaucoma
Occasional (5-29%)HP:0000501
Visual loss
Occasional (5-29%)HP:0000572
Anterior uveitis
Very rare (1-4%)HP:0012122
Cataract
HP:0000518
Optic atrophy
HP:0000648
Optically empty vitreous
HP:0030663
Partial loss of field of vision
HP:0001123
Peripheral traction retinal detachment
HP:0007643
Retinal pigment epithelial atrophy
HP:0007722
Vitreoretinopathy
HP:0007773
Related Conditions
Quick Facts
- SNOMED CT
- 232064001
- UMLS CUI
- C1840452
- Fully Specified Name
- Wagner syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 20
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.